RECENT product recalls

The Hillshire Brands Company Recalls Corn Dog and Sausage On A Stick Products Due To Possible Extraneous Matter Contamination

March 17, 2025, and September 26, 2025.

Necessary Information:

Company Announcement:

WASHINGTON, September 27, 2025 – The Hillshire Brands Company, a Haltom City, Tex. establishment, is recalling approximately 58,000,000 pounds of corn dog and sausage on a stick products that may be contaminated with extraneous material, specifically pieces of wood embedded in the batter, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The corn dog and sausage on a stick products were packaged between March 17, 2025, and September 26, 2025. A list of the products subject to recall can be found here: [view product list]. The labels for the impacted products can be found here: [view labels].

The products subject to recall bear establishment number “EST-582” or “P-894” printed on the packaging. These items were sold online and shipped to retail and food service locations nationwide. They were also sold to school districts and Department of Defense facilities nationwide. While the products were distributed to schools, it resulted from commercial sales and not part of food provided by the USDA for the National School Lunch Program.

The problem was discovered after the establishment received multiple consumer complaints, five of which involved injuries. The Hillshire Brands Company conducted an investigation and determined that the wooden sticks entered the production process prior to product battering. FSIS has received no additional reports of injury from consumption of these products. Anyone concerned about an injury should contact a healthcare provider.

FSIS is concerned that some products may be in consumers’ refrigerators and freezers, along with school and institution refrigerators and freezers. Consumers, schools, and institutions who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers with questions about the recall can contact Christina Self, The Hillshire Brands Company Associate Director of Customer Care, at 888-747-7611. Members of the media with questions about the recall can contact MaKenzie Taylor, The Hillshire Brands Company Communications Manager, at 810-391-6680.

Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Necessary Information:

Web Link- https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-ready-eat-meals-containing-pasta-may-be-contaminated

See original announcement for examples of labels

Company Announcement:

WASHINGTON, September 25, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat meals containing a Food and Drug Administration (FDA) regulated pre-cooked pasta that may be contaminated with Listeria monocytogenes (Lm). FSIS expects more updates as this investigation continues. As more information becomes available, FSIS will update this public health alert. Consumers should check back frequently because additional products may be added.

The following product is subject to the public health alert [view labels]:

12-oz. clear plastic tray packages labeled “MARKETSIDE LINGUINE WITH BEEF MEATBALLS & MARINARA SAUCE” with “best if used by” dates SEP 22, 2025; SEP 24, 2025; SEP 25, 2025; SEP 29, 2025; SEP 30, 2025; and OCT 01, 2025.

The product bears establishment number “EST. 50784” or "EST. 47718" inside the USDA mark of inspection. This item was shipped to Walmart locations nationwide.

The producing company collected samples of the FDA-regulated, pre-cooked pasta used as an ingredient in these products as part of the ongoing investigation related to the Listeria outbreak linked to chicken fettuccine alfredo meals. The test confirmed that the linguine pasta was positive for Lm and further testing is ongoing to determine if the Lm is genetically related to the specific outbreak strain. FSIS previously issued a recall notice linked to the Listeria outbreak in June and continues to coordinate with FDA, the Centers for Disease Control and Prevention, and state public health partners.

Consumption of food contaminated with Lm can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.

Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.

FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

Consumers with questions regarding the public health alert can contact Nate’s Fine Foods at 916-677-7303. Operating hours are between 9:00 a.m. and 4:00 p.m. PST Monday through Friday.

Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Kroger bagged frozen shrimp and Kroger frozen shrimp products

Necessary Information:

Web Link- https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lawrence-wholesale-llc-recalls-kroger-bagged-frozen-shrimp-and-kroger-frozen-shrimp-products-because

See original announcement for examples of labels

Company Announcement:

Lawrence Wholesale LLC of Vernon, CA is recalling a limited quantity of Kroger bagged frozen shrimp and Kroger frozen shrimp products because they may have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with Cesium-137 (Cs-137).

Cs-137 is a man-made radioisotope of cesium. Traces of Cs-137 are widespread and can be present in the environment at background levels, and at higher levels in water or foods grown, raised, or produced in areas with environmental contamination. The primary health effect of concern following longer term, repeated low dose exposure (e.g., through consumption of contaminated food or water over time) is an elevated risk of cancer, resulting from damage to DNA within living cells of the body.

Bagged frozen shrimp and shrimp cocktail products were sold by Kroger in the following states: AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN, KS, KY, LA, MI, MO, MS, MT, NE, NM, NV, OH, OR, SC, TN, TX, UT, VA, WA, WI, WV and WY. The product has the following descriptions and codes:

Item Description 

UPC 

Lot Number 

Best By Date 

Shrimp Bowl

Cooked Shrimp with

Cocktail Sauce (7oz)

011110622952

11325-H3A1

11425-H3A1

11525-H3A1

11625-H3A1

04/22/2027 

04/23/2027 

04/24/2027

04/25/2027

Shrimp Cocktail with

Cocktail Sauce

(17oz)

011110624840

13725-H3A1

13825-H3A1

05/16/2027 

05/17/2027

Kroger Cooked

Jumbo Tail-On,

Peeled & Deveined

16/25 Shrimp

011110649812

11925-H3A1

12025-H3A1

04/28/2027

04/29/2027

Kroger Cooked

Medium Tail-On,

Peeled & Deveined

51/60 Shrimp

011110967015

12225-H3A1

12325-H3A1

05/01/2027

05/02/2027

The FDA is actively investigating reports of Cs-137 contamination in shipping containers and frozen shrimp products manufactured in Indonesia by PT. Bahari Makmur Sejati (doing business as BMS Foods). No illnesses have been reported to date. As noted in the FDA statement issued on 8/19/25: “At this time, no product that has tested positive or alerted for Cesium-137 (Cs-137) has entered the U.S. commerce.”

FDA is working with distributors and retailers that received product from PT. Bahari Makmur Sejati after the date of first detection of Cs-137 by Customs & Border Protection (CBP), but from shipments that did not alert for Cs-137, to recommend that firms conduct a recall. In conjunction with other information, FDA determined that product from PT. Bahari Makmur Sejati violates the Federal Food, Drug, & Cosmetic Act in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with Cs-137 and may pose a safety concern.

Consumers who have purchased the recalled bagged frozen shrimp or frozen shrimp products should not consume the product and should dispose of the product or return it to the place of purchase for a full refund. Consumers with questions may contact the company at (323) 235-7535, Monday to Friday from 9:00 am to 4:00 pm PT.

This recall is being made with the knowledge of the U.S. Food and Drug Administration.

Readt to eat tirkey gobbler wrap

Necessary Information:

Web Link- https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-ready-eat-turkey-wrap-product-due-possible-listeria

See original announcement for examples of labels

Company Announcement:

WASHINGTON, September 19, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for a ready-to-eat (RTE) turkey wrap product due to concerns that the product may be contaminated with Listeria monocytogenes. A recall was not requested because the affected product is no longer available for purchase.

The RTE turkey wrap product was produced on September 10, 2025. The following product is subject to the public health alert [view sample labels]:

10-oz. clear plastic clamshell packages containing “TRADER JOE’S TURKEY GOBBLER WRAP” with “BEST BY SEP 16, 2025.”

The product bears establishment number “P-1644” inside the USDA mark of inspection. This item was shipped to Trader Joe’s retail locations nationwide.

The problem was discovered when the establishment notified FSIS that food contact surface samples associated with this product tested positive for Listeria monocytogenes.

There have been no confirmed reports of adverse reactions due to consumption of this product. Anyone concerned about an illness should contact a health care provider.

Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.

Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.

FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased this product are urged not to consume it. The product should be thrown away or returned to the place of purchase.

Media and consumers with questions regarding the public health alert can contact Trader Joe’s Customer Relations at 626-599-3817, on Monday through Friday from 6:00 am to 6:00 pm Pacific Time.

Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/

Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp.

Necessary Information:

Company Announcement:

September 19, 2025, AquaStar (USA) Corp of Seattle, WA is recalling: 

approximately 49,920 bags (net wt. 2lbs) of Kroger Raw Colossal EZ Peel Shrimp.

approximately 18,000 bags (net wt. 2lbs) of Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp.

approximately 17,264 bags (net wt. 1.25lbs) of AquaStar Raw Peeled Tail-on Shrimp Skewers because they may have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with cesium-137 (Cs-137).

Cs-137 is a man-made radioisotope of cesium. Traces of Cs-137 are widespread and can be present in the environment at background levels, and at higher levels in water or foods grown, raised, or produced in areas with environmental contamination. The primary health effect of concern following longer term, repeated low dose exposure (e.g., through consumption of contaminated food or water over time) is an elevated risk of cancer, resulting from damage to DNA within living cells of the body.

The affected shrimp was sold at Baker’s, City Market, Dillons, Food 4 Less, Foodsco, Fred Meyer, Fry’s, Gerbes, Jay C, King Soopers, Kroger, Mariano’s, Metro Market, Pay Less Supermarkets, Pick ‘n Save, Ralphs, Smith’s and QFC in AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN, KS, KY, LA, MI, MO, MS, MT, NE, NM, NV, OH, OR, SC, TN, TX, UT, VA, WA, WI, WV and WY between June 12, 2025 and September 17, 2025.

The recalled Kroger Raw Colossal EZ Peel Shrimp net wt. 2lbs., is packaged in transparent printed bag with a blue band on the top with yellow and red details, and has the following codes:

  • UPC 20011110643906, lot code 10662 5085 10, Best If Used By: 03 26 27

  • UPC 20011110643906, lot code 10662 5097 11, Best If Used By: 04 07 27

  • UPC 20011110643906, lot code 10662 5106 11, Best If Used By: 04 16 27

  • UPC 20011110643906, lot code 10662 5107 10, Best If Used By: 04 17 27

  • UPC 20011110643906, lot code 10662 5111 11, Best If Used By: 04 21 27

  • UPC 20011110643906, lot code 10662 5112 10, Best If Used By: 04 22 27

  • UPC 20011110643906, lot code 10662 5113 10, Best If Used By: 04 23 27

  • UPC 20011110643906, lot code 10662 5113 11, Best If Used By: 04 23 27

  • UPC 20011110643906, lot code 10662 5114 10, Best If Used By: 04 24 27

  • UPC 20011110643906, lot code 10662 5114 11, Best If Used By: 04 24 27

The recalled Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp, net wt. 2lbs., is packaged in clear plastic bag and has a white label with green stripes on top of each bag and has the following codes:

  • UPC 011110626196, lot code 10662 5112 11, Best Before: 10 22 2027

  • UPC 011110626196, lot code 10662 5113 10, Best Before: 10 23 2027

The recalled AquaStar Raw Peeled Tail-on Shrimp Skewers; net wt. 1.25 lbs., is packaged in a printed bag with a black top and blue bottom and printed pictures of the skewers inside, and has the following codes:

  • UPC 731149390010, lot code 10662 5127 10, Best If Used By: 11 07 2027

  • UPC 731149390010, lot code 10662 5128 11, Best If Used By: 11 08 2027

  • UPC 731149390010, lot code 10662 5133 11, Best If Used By: 11 13 2027

  • UPC 731149390010, lot code 10662 5135 10, Best If Used By: 11 15 2027

The FDA is actively investigating reports of Cesium-137 (Cs-137) contamination in shipping containers and frozen shrimp products processed by PT. Bahari Makmur Sejati (doing business as BMS Foods) of Indonesia. No illnesses have been reported to date. As noted in the FDA statement issued on 8/19/25: “At this time, no product that has tested positive or alerted for Cesium-137 (Cs-137) has entered the U.S. commerce.”

“FDA is working with distributors and retailers that received product from PT. Bahari Makmur Sejati after the date of first detection of Cs-137 by Customs & Border Protection (CBP), but from shipments that did not alert for Cs-137, to recommend that firms conduct a recall. In conjunction with other information, FDA determined that product from PT. Bahari Makmur Sejati violates the Federal Food, Drug, & Cosmetic Act in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with Cs-137 and may pose a safety concern.”

Consumers who have purchased affected shrimps should not consume the product and should dispose of or return it to the place of purchase for a full refund.

Consumers with questions may contact the company at 1-800-331-3440, Monday-Friday, 8am-5 pm PST.

This recall is being made with the knowledge of the U.S. Food and Drug Administration

Kirkland Signature brand Ahi Tuna Wasabi Poke

Necessary Information:

Web Link- https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/western-united-fish-company-recalls-kirkland-signature-brand-ahi-tuna-wasabi-poke-because-possible

See original announcement for examples of labels

Company Announcement:

September 20, 2025, Western United Fish Company dba Annasea Foods Group of Kent, WA is recalling 3,314.7 lbs. of Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco Item Number of 17193, with the Sell By Date of 9/22/2025, because the green onions used in the product have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can lead to serious pregnancy complications among pregnant women.

The affected Ahi Tuna Wasabi Poke product is packaged in clear plastic clamshell containers and has the Kirkland Signature brand label with the Pack Date of 9/18/2025 and Sell By Date of 9/22/2025.

Product was sold at the deli section from Costco Warehouse stores in the following states on 9/18/2025: Alabama, Alaska, Colorado, Connecticut, Delaware, Florida, Georgia, Idaho, Indiana, Louisiana, Maine, Maryland, Massachusetts, Minnesota, Mississippi, Missouri, Montana, Nebraska, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, and Wisconsin.

No illnesses have been reported to date.

This recall was initiated after being notified by our green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi Tuna Wasabi Poke on 9/17/2025. We are continuing to work with our green onion supplier to determine the root cause.

Consumers should not consume this affected product and dispose of it immediately and visit your local Costco for a full refund.

Please call Western United Fresh Co. DBA Annasea Foods Group at (425) 558-7809, 7:00am - 3:30pm Pacific Time, Monday – Friday, or email info@annasea.com if you have any issues or concerns.

This recall is being made with the knowledge of the U.S. Food and Drug Administration.

Sprout Organics® Sweet Potato Apple and Spinach

Necessary Information:

Web Link- https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sprout-organics-voluntarily-recalls-one-lot-sweet-potato-apple-and-spinach-due-possible-health-risk

See original announcement for examples of labels

Company Announcement:

Sprout Organics has initiated a voluntary recall of one lot of Sprout Organics® Sweet Potato Apple and Spinach because it may contain elevated levels of lead.

Exposure to lead, even at low levels, may increase blood lead levels. Additional signs and symptoms of lead exposure are more likely with acute exposure to higher levels of lead or chronic exposure to lead. The effects of lead depend upon the amount and duration of exposure and age/body weight. If a child is exposed to enough lead for a protracted period of time, this can affect learning and development or cause other long-term health problems.

The product, a 3.5-ounce pouch, was sold in Walgreens and some independent stores in the US South region with most sales occurring between September and December 2024. The product was not sold in any other large grocery chain besides Walgreens.

If consumers have product matching the following description in their possession, they should return it to their local store for a full refund. The lot code and expiration date are printed on the bottom strip on the back of the pouch (see photos attached).

Product Name 

Purchased From 

Lot Code 

Expiration Date 

Sprout Organics® Sweet

Potato Apple and Spinach

3.5 oz pouch

Walgreens and independent

stores in US South region

4212

10/29/2025

No illnesses have been reported to date and no other Sprout Organics products are impacted by this voluntary recall. The voluntary recall is being initiated after routine sampling.

To learn about Sprout Organics comprehensive testing program of ingredients and products before distribution, please go to https://sproutorganics.com/pages/faqExternal Link Disclaimer.

Consumers with questions should contact the company at 510-833-6089 Monday through Friday 9 am to 5 pm Pacific Time or by email at Info@sproutorganics.com.


RECALL Good & Gather Southwest-Style Burrito Bowl Blend

Necessary Information:

Web Link- https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/one-frozen-llc-voluntarily-recalls-good-gathertm-southwest-style-burrito-bowl-blend-frozen-12oz-bags

See original announcement for examples of labels

Company Announcement:

One Frozen, LLC of Rochester, NY, is voluntarily recalling certain lots of Good & Gather™ Southwest-Style Burrito Bowl Blend (frozen, 12oz bags) because the product may contain shrimp (crustacean shellfish) that was not declared on the ingredient label of the product. People who have an allergy or severe sensitivity to shellfish run the risk of a serious or life-threatening allergic reaction if they consume this product.

Good & Gather™ Southwest-Style Burrito Bowl Blend were distributed through Target retail stores nationwide, in all 50 states. The distribution from One Frozen, LLC to Target began on 4/17/2025.

Product Identification:

Product Name: Good & Gather™ Burrito Bowl Blend, Southwest-Style (Frozen)

Package Size: 12 oz (340g) bags

UPC: 085239931356 – Lot codes can be found under the Nutrition Label on the back of the packaging

Lot Codes: L5055-1, L5055-2, L5055-3, L5055-4, L5055-5, and L5055-6

Best if Used by Date: 08/24/2026

Quantity Distributed: 57,240 consumer units

The recall is being initiated after three consumer complaints were received indicating the possible presence of shrimp in this product. No illness have been reported as of September 10, 2025.

This recall is being conducted in cooperation with the U.S. Food and Drug Administration (FDA).

What Consumers Should Do:

Check your freezer for the affected product.

If you purchased the Good & Gather™ Southwest-Style Burrito Bowl Blend, 12 oz bag with lot codes L5055-1, L5055-2, L5055-3, L5055-4, L5055-5, and L5055-6, do not consume this product and contact Target Guest Relations at (800) 440-0680 for a full refund.

Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp recall

****RECALL****

MISSOURI DEPARTMENT OF HEALTH AND SENIOR SERVICES RECALL ALERT

Necessary Information:

• Web Link- https://www.fda.gov/.../aquastar-usa-corp-recalls-kroger...

• See original announcement for examples of labels

Company Announcement

August 27, 2025, AquaStar (USA) Corp of Seattle, WA is recalling approximately 18,000 bags (net wt. 2lbs) of Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp because they may have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with cesium-137 (Cs-137).

Cs-137 is a man-made radioisotope of cesium. Traces of Cs-137 are widespread and can be present in the environment at background levels, and at higher levels in water or foods grown, raised, or produced in areas with environmental contamination. The primary health effect of concern following longer term, repeated low dose exposure (e.g., through consumption of contaminated food or water over time) is an elevated risk of cancer, resulting from damage to DNA within living cells of the body.

The affected shrimp was sold at Baker’s, Gerbes, Jay C, Kroger, Mariano’s, Metro Market, Pay Less Supermarkets, and Pick ‘n Save in AL, AR, GA, IL, IN, KS, KY, MI, MO, MS, NE, OH, SC, TN, VA, WI, WV between July 24, 2025 and August 11, 2025.

The recalled Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp, net wt. 2lbs., is packaged in clear plastic bag and has a white label with green stripes on top of each bag and has the following codes:

• UPC 011110626196, Lot code 10662 5139, Best Before 11/19/2027

• UPC 011110626196, Lot code 10662 5140, Best Before 11/20/2027

The FDA is actively investigating reports of Cesium-137 (Cs-137) contamination in shipping containers and frozen shrimp products processed by PT. Bahari Makmur Sejati (doing business as BMS Foods) of Indonesia. No illnesses have been reported to date. As noted in the FDA statement issued on 8/19/25: “At this time, no product that has tested positive or alerted for Cesium-137 (Cs-137) has entered the U.S. commerce.”

“FDA is working with distributors and retailers that received product from PT. Bahari Makmur Sejati after the date of first detection of Cs-137 by Customs & Border Protection (CBP), but from shipments that did not alert for Cs-137, to recommend that firms conduct a recall. In conjunction with other information, FDA determined that product from PT. Bahari Makmur Sejati violates the Federal Food, Drug, & Cosmetic Act in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with Cs-137 and may pose a safety concern.”

Consumers who have purchased affected shrimps should not consume the product and should dispose of or return it to the place of purchase for a full refund.

Consumers with questions may contact the company at 1-800-331-3440, Monday-Friday, 8am-5 pm PST.

This recall is being made with the knowledge of the U.S. Food and Drug Administration.

Taylor Farms Honey Balsamic Salad Kit recall

****RECALL****

Necessary Information:

• Web Link- https://www.fda.gov/.../company-voluntarily-recalls-honey...

• See original announcement for examples of labels

Company Announcement:

Salinas, Calif., August 26, 2025 – In response to a recall initiated by Latitude 36 Foods, LLC., Taylor Fresh Foods is voluntarily recalling the Taylor Farms Honey Balsamic Salad Kit 6/8.3oz. because it may contain undeclared sesame and soy allergens. People who have an allergy or severe sensitivity to sesame and soy run the risk of serious or life-threatening allergic reaction if they consume these products.

Master packs — individual packets of dressing and toppings supplied by Latitude 36 Foods and included in Taylor Farms salad kits — incorrectly included Asian Sesame Ginger dressing rather than the intended Honey Balsamic Vinaigrette dressing, leading to the possibility of undeclared sesame and soy allergens in some Taylor Farms Honey Balsamic Salad Kits.

The Taylor Farms Honey Balsamic Salad Kit 6/8.3oz in scope of this recall was distributed in AL, AZ, CA, CO, DE, FL, GA, IN, KS, KY, LA, MI, MO, MS, NJ, NY, OH, OR, PA, TN, TX, UT, VA, WA and WV and has code dates starting with “TFRS” and “Best If Used By” date up to and including September 4, 2025. The product code can be found in the upper right-hand corner of the packaging.

Consumers who have the recalled salad kit should discard it immediately and not consume it. Refunds are available at the location of purchase. There have been no illnesses reported to Taylor Farms in connection with the recalled product. This recall does not apply to any other Taylor Farms products or brands. Consumers with any questions may contact our customer care team at 855-455-0098 Monday through Friday from 8am-5pm PT.

• Distribution information:

This product was distributed to the following Walmart stores

Address

City

State

Zip Code

1310 PREACHER ROE BLVD

WEST PLAINS

MO

65775-2938

333 S WESTWOOD BLVD

POPLAR BLUFF

MO

63901-5519

2050 W 76 COUNTRY BLVD

BRANSON

MO

65616-2100

1500 1ST ST

KENNETT

MO

63857-2522

1401 OLD EXETER ROAD

CASSVILLE

MO

65625-9415

18401 STATE HWY 13

BRANSON WEST

MO

65737-0000

1101 BRANSON HILLS PKWY

BRANSON

MO

65616-9942

100 COMMERCIAL LN

PINEVILLE

MO

64856-7069

3001 OAK GROVE ROAD

POPLAR BLUFF

MO

63901-0000


blue bell icecream recall

****RECALL****

Necessary Information:

• Web Link- https://www.fda.gov/.../blue-bell-ice-cream-issues...

• See original announcement for examples of labels

Company Announcement:

BRENHAM, Texas, August 22, 2025 – Blue Bell Ice Cream is voluntarily recalling a limited quantity of Moo-llennium Crunch Ice Cream half gallon packaged in a Chocolate Chip Cookie Dough carton produced in its Brenham, Texas, plant because of undeclared almond, walnut, and pecan. The recalled product was mistakenly packaged in Chocolate Chip Cookie Dough ice cream cartons with a Moo-llennium Crunch lid. People who have an allergy or severe sensitivity to almonds, walnuts, and pecans run the risk of a serious or life-threatening allergic reaction if they consume these products.

A Blue Bell employee discovered the incorrect packaging on two half gallons while restocking a retailer. No illnesses or adverse reactions have been reported to date. No other incorrect packaging has been discovered or reported to date.

The half gallons can be identified as Moo-llennium Crunch Ice Cream packaged in a Chocolate Chip Cookie Dough half gallon carton with a Moo-llennium Crunch lid and with the following code located on the top of the half gallon lid: 061027524. An image of the affected product is included below.

The affected ice cream half gallons were distributed through retail outlets in Alabama, Arkansas, Florida Panhandle, Northwest Georgia, Southern Indiana, Southern Illinois, Kansas, Kentucky, Louisiana, Mississippi, Missouri, New Mexico, Oklahoma, Tennessee, Texas, and Southwest Virginia.

Consumers who have purchased these items can return them to the place of purchase for a full refund.

For more information, consumers may call 979-836-7977, Monday – Friday 8 a.m. – 5 p.m. CST or email us at consumerrelations@bluebell.com.

This recall is being made with the knowledge of the U.S. Food and Drug Administration.

RECALL Raw Frozen Shrimp PT. Bahari Makmur Sejati (doing business as BMS Foods)

Necessary Information:

Company Announcement:

Product and stores affected 

Certain raw frozen shrimp products processed by PT. Bahari Makmur Sejati (doing business as BMS Foods), a company located in Indonesia, and sold at Walmart. 

These products include the following product names, lot codes, and best by dates: 

  • Great Value brand frozen raw shrimp, lot code: 8005540-1, Best by Date: 3/15/2027

  • Great Value brand frozen raw shrimp, lot code: 8005538-1, Best by Date: 3/15/2027

  • Great Value brand frozen raw shrimp, lot code: 8005539-1, Best by Date: 3/15/2027

Additional product information is in a table below.  

At this time, no product that has tested positive or alerted for Cesium-137 (Cs-137) has entered the U.S. commerce. FDA is working with distributors and retailers that received product from PT. Bahari Makmur Sejati after the date of first detection of Cs-137 by Customs & Border Protection (CBP), but from shipments that did not alert for Cs-137, to recommend that firms conduct a recall. In conjunction with other information, FDA determined that product from PT. Bahari Makmur Sejati violates the Federal Food, Drug, & Cosmetic Act in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with Cs-137 and may pose a safety concern. 

FDA has also added PT. Bahari Makmur Sejati to a new import alert for chemical contamination to stop products from this firm from coming into the U.S. until the firm has resolved the conditions that gave rise to the appearance of the violation.

FDA’s investigation is ongoing. This advisory will be updated as more information becomes available. 

Health impacts of cesium exposure

FDA detected Cs-137 in a single shipment of imported frozen shrimp from PT. Bahari Makmur Sejati that did not enter U.S. commerce. The level of Cs-137 detected in the detained shipment was approximately 68 Bq/kg, which is below FDA’s Derived Intervention Level for Cs-137 of 1200 Bq/kg. At this level, the product would not pose an acute hazard to consumers. Avoiding products like the shipment FDA tested with similar levels of Cs-137 is a measure intended to reduce exposure to low-level radiation that could have health impacts with continued exposure over a long period of time.

The primary health effect of concern following longer term, repeated low dose exposure (e.g., through consumption of contaminated food or water over time) is an elevated risk of cancer, resulting from damage to DNA within living cells of the body. Additional information about Cs-137 and your health is available through the Centers for Disease Control and Prevention’s Agency for Toxic Substances and Disease Registry resources.

Recommendation

  • If you recently purchased one of the impacted lots of Great Value raw frozen shrimp from Walmart, throw it away. Do not eat or serve this product.

  • Distributors and retailers should dispose of this product and should not sell or serve this product.

  • If you suspect you have been exposed to elevated levels of cesium, talk to your healthcare provider.

 

Current Update

August 19, 2025

FDA is actively investigating reports of Cesium-137 (Cs-137) contamination in shipping containers and frozen shrimp products processed by PT. Bahari Makmur Sejati (doing business as BMS Foods) of Indonesia. The U.S. Customs & Border Protection (CBP) alerted FDA to the detection of Cs-137 in shipping containers at four U.S. ports (Los Angeles, Houston, Savannah, and Miami). FDA collected multiple samples for radionuclide analysis, with results confirming the presence of Cs-137 in one sample of breaded shrimp. All containers and product testing positive or alerting for Cs-137 have been denied entry into the country. The agency continues to coordinate with CBP to prevent any contaminated products from reaching consumers and is working with Indonesian seafood regulatory authorities to investigate the root cause of the contamination. 

Although testing to date has not confirmed the presence of contamination in any product in commerce, the product appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with Cs-137 and may pose a safety concern. To date, FDA has learned that Walmart has received implicated raw frozen shrimp, imported after the date of first detection of Cs-137 by CBP, but from shipments that did not alert for Cs-137. FDA has recommended Walmart recall this product. 

Consumers should not eat or serve certain lots of Great Value raw frozen shrimp from Walmart: 

  • Great Value brand frozen raw shrimp, lot code: 8005540-1, Best by Date: 3/15/2027 

  • Great Value brand frozen raw shrimp, lot code: 8005538-1, Best by Date: 3/15/2027 

  • Great Value brand frozen raw shrimp, lot code: 8005539-1, Best by Date: 3/15/2027. 

If you have recently purchased raw frozen shrimp from Walmart that matches this description, throw it away. Do not eat or serve this product.

Cs-137 is a radioisotope of cesium that is man-made through nuclear reactions and because it is widespread worldwide, trace amounts of Cs-137 can be found in the environment, including soil, food, and air. FDA food monitoring focuses on radioisotopes (radionuclides) that are not normally present and are generally the result of human activities. Any unexpected finding of Cs-137 in a food product is evaluated to determine if follow up action is warranted on a case-by-case basis. After being alerted to the contamination of shipping containers detected by CBP, FDA initiated sampling of products which included five different shrimp products from PT. Bahari Makmur Sejati, one of which was a sample of frozen breaded shrimp. FDA's laboratory confirmation of Cs-137 in the breaded shrimp had detectable levels of Cs-137 present at 68.48 Bq/kg +/- 8.25 Bq/kg. There was no detectable Cs-137 in the other products tested; however, this does not rule out contamination.

FDA has not detected Cs-137 in any product above the current derived intervention levels for Cs-137 (1200 Bq/kg); however, FDA has concluded that the level detected in the breaded shrimp sample could represent a potential health concern for those exposed to this level of Cs-137 from consumption of the shrimp over an extended period of time combined with radiation that exists in the environment and from other sources such as medical procedures. Avoiding products like the shipment FDA tested with similar levels of Cs-137 is a measure intended to reduce exposure to low-level radiation that could have health impacts with continued exposure over a long period of time. FDA has taken swift action to prevent potentially contaminated product from being introduced into U.S. commerce in response to reports of contaminated shipping containers from CBP. On August 14, 2025, FDA posted a new import alert (IA 99-51) for chemical contamination under section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act. PT. Bahari Makmur Sejati has been added to the red list of this alert due to the presence of Cs-137. The import alert ensures that no implicated shrimp products will enter U.S. commerce until the company resolves the conditions that gave rise to the appearance of the violation. 

FDA will continue working with industry to trace all implicated products processed by PT. Bahari Makmur Sejati through the supply chain to gather as much information about them as possible and take action as appropriate. Product information will be added to this advisory as it becomes available.

Product Descriptions

Brand

Product Name

Product Type

Best By

Item Code

Lot Code

Distributor

Great Value

Frozen Raw White Vannamei Shrimp

Frozen Raw Ez Peel Tail-On Farm-Raised White Vannamei Shrimp, 2lb bag

3/15/2027

7383108

8005540-1

Walmart

Great Value

Frozen Raw White Vannamei Shrimp

Frozen Raw Ez Peel Tail-On Farm-Raised White Vannamei Shrimp, 2lb bag

3/15/2027

7383108

8005538-1

Walmart

Great Value

Frozen Raw White Vannamei Shrimp

Frozen Raw Ez Peel Tail-On Farm-Raised White Vannamei Shrimp, 2lb bag

3/15/2027

7383108

8005539-1

Walmart

Useful Links

Clover Valley Instant Coffee Recall

• Web Link- https://www.fda.gov/.../dollar-general-announces...

• See original announcement for examples of labels

Company Announcement:

Goodlettsville, Tennessee – August 11, 2025 –Dollar General Corporation is recalling three (3) lots of its eight ( ounce Clover Valley® Instant Coffee due to the potential presence of glass.

8-Ounce Clover Valley® Instant Coffee

Package UPC: 876941004069

Lot: L-5163 / Best By 12/13/2026

Lot: L-5164 / Best by 12/13/2026

Lot: L-5165 / Best by 12/14/2026

Customers can find the lot and best by date information around the neck of the unit.

Clover Valley® Instant Coffee was sold and distributed between July 9-21, 2025 exclusively in Dollar General retail stores located in the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA,ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI ,WV, and WY.

The recall is being initiated after a customer notified Dollar General employees about the potential issue. Ingesting glass fragments may cause injury to the consumer, and these injuries may include damage to teeth, laceration of the mouth and throat, or perforation of the intestine. No illnesses or injuries have been reported to date.

Customers who purchased this product are encouraged to discard it and contact Dollar General either via email at customercare@dollargeneral.com or by phone at 1-888-309-9030 from 6 a.m. to 1 a.m. CST seven days a week to request a full refund of the purchase price (including any tax).

Dollar General is actively investigating the source of the glass contamination and apologizes for any inconvenience caused by this product issue. The recall is being conducted with the knowledge of the U.S. Food & Drug Administration (FDA).

For additional information, please contact the Media Relations Department at dgpr@dg.com.

About Dollar General Corporation Dollar General Corporation

(NYSE: DG) is proud to serve as America’s neighborhood general store. Founded in 1939, Dollar General lives its mission of Serving Others every day by providing access to affordable products and services for its customers, career opportunities for its employees, and literacy and education support for its hometown communities. As of May 2, 2025, the Company’s 20,582 Dollar General, DG Market, DGX and pOpshelf stores across the United States and Mi Súper Dollar General stores in Mexico provide everyday essentials including food, health and wellness products, cleaning and laundry supplies, self-care and beauty items, and seasonal décor from our high-quality private brands alongside many of the world’s most trusted brands such as Coca Cola, PepsiCo/Frito-Lay, General Mills, Hershey, J.M. Smucker, Kraft, Mars, Nestlé, Procter & Gamble and Unilever.

DermaRite Industries recall

Necessary Information:

· Web Link- https://www.fda.gov/.../dermarite-industries-issues...

· See original announcement for examples

Company Announcement

DermaRite Industries, LLC is voluntarily recalling individual lots of products in the table below due to microbial contamination identified as Burkholderia cepecia.

Risk Statement: Burkholderia Cepacia Complex in these products may result in serious and life-threatening infections. The contaminated products may be used by immunosuppressed individuals or by people attending to immunosuppressed individuals. In healthy individuals with minor skin lesions the use of the product will more likely result in local infections, whereas in immunocompromised individuals the infection is more likely to spread into blood stream leading to life-threatening sepsis. To date, DermaRite has not received any reports of adverse events related to this recall.

DermaKleen is an OTC Healthcare antiseptic lotion soap with Vitamin E indicated for handwashing to decrease bacteria on the skin.

DermaSarra is an OTC External analgesic indicated for temporary relief of itching associated with minor skin irritations due to: dry skin, insect bites, detergents, sunburn.

KleenFoam is an OTC Antimicrobial foam soap with Aloe Vera indicated for handwashing to decrease bacteria on the skin after changing diapers, after assisting ill people, or before contact with a person under medical care or treatment.

PeriGiene is an OTC Antiseptic cleanser indicated for use in the perineal area.

The recalled products were distributed nationwide in the United States and in Puerto Rico.

Recalled Product Information: (see Table image below)

DermaRite has notified its distributors and customers by e-mail to immediately examine available inventory and destroy all affected products in accordance with each facility’s process.

Consumers with questions regarding this recall can call Mary Goldberg at 973-569-9000 x104 Monday through Friday, 9:00 am – 5:00 pm EST or email voluntary.action@dermarite.com.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail, or by fax.

• Complete and submit the report online: www.fda.gov/medwatch/report.htm

• Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form or submit by fax to 1-800-FDA-0178.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Company Contact Information

Consumers:

Mary Goldberg

973-569-9000 x104

voluntary.action@dermarite.com