All Product Recalls

Browse through 2,313 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

HIGHFDA FOOD

Giant Eagle Recalls Smoked Mozzarella Penne Salad Over Listeria Risk

Giant Eagle recalled 16 pounds of Smoked Mozzarella Penne Salad on October 2, 2025, due to potential listeria contamination. The affected product was sold in Pennsylvania, Ohio, Indiana, and Maryland. Consumers should not consume the product and contact the company for refunds.

Giant Eagle
Recall notification
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HIGHFDA FOOD

Leprino Foods Recalls Mozzarella Due to Metal Contamination

Leprino Foods recalled over 5.4 million pounds of mozzarella cheese on October 2, 2025, due to possible stainless steel contamination. The recall affects products distributed in Ohio, Tennessee, Texas, Utah, and Wisconsin. Consumers should not consume the product and should seek a refund.

Leprino Foods
Possible stainless
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HIGHFDA DRUG

ZICAM Medicated Fruit Drops Recalled Due to Labeling Error

Church & Dwight Co., Inc. recalled 21,912 bottles of ZICAM Medicated Fruit Drops on October 1, 2025. The recall stems from a labeling mix-up that failed to disclose elderberry as an ingredient. Consumers should stop using the product immediately.

ZICAM COLD REMEDY MEDICATED FRUIT DROPS - ELDERBERRY
Labeling: Label
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HIGHFDA FOOD

Demers Food Group Recalls Shrimp Scampi Due to Listeria Risk

Demers Food Group recalled 12,962 cases of Scott & Jon's Shrimp Scampi with Linguine on October 1, 2025. The product may contain linguine linked to Listeria monocytogenes. Consumers should not consume it and seek a refund.

DEMERS FOOD GROUP
Contains Linguine
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HIGHFDA DEVICE

SHENZHEN ATOMSTACK TECHNOLOGIES Recalls Laser Products Over Safety Hazard

SHENZHEN ATOMSTACK TECHNOLOGIES recalled material processing laser products on September 30, 2025, due to a missing remote interlock connector. This defect poses a high risk according to federal regulations. Consumers should stop using these devices immediately and follow manufacturer instructions for remedy.

SHENZHEN ATOMSTACK TECHNOLOGIES
Lack of
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HIGHFDA DEVICE

B BRAUN MEDICAL Recalls Hemodialysis Bloodlines Over Air Bubble Risk

B BRAUN MEDICAL recalled 1,298,454 hemodialysis bloodlines on September 30, 2025. The recall results from the risk of micro-air bubbles due to damaged connectors. Patients should stop using the product immediately and follow the manufacturer’s instructions.

B BRAUN MEDICAL
The potential
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HIGHFDA FOOD

New Age International Recalls Enoki Mushroom Over Listeria Risk

New Age International, Inc. recalled 175 boxes of its Signature brand Enoki Mushroom on September 29, 2025. The product may be contaminated with Listeria monocytogenes, which poses serious health risks. Consumers should not eat the product and seek a refund or replacement.

New Age International
Product may
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HIGHFDA DRUG

Medline Recalls Alcohol Prep Pads Due to Subpotency Risk

Medline Industries recalled 222,800 boxes of alcohol prep pads on September 29, 2025. The recall follows concerns the product may not meet potency standards. Consumers must stop using the pads and seek guidance from healthcare providers.

Medline Industries, LP
Subpotent Drug
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HIGHFDA DEVICE

Philips Medical Systems Recalls Zenition 50 X-Ray Systems Due to Imaging Issues

Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 x-ray systems on September 29, 2025. The devices may suffer from corrosion of the Image Intensifier Television control board, leading to poor image quality. Users must stop using the device immediately and follow the recall instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Over time
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HIGHFDA DRUG

Acuity Specialty Products Recalls Hand Sanitizer Due to Methanol Risk

Acuity Specialty Products recalled its Wyandotte Sanifect E3 hand sanitizer on September 29, 2025. The recall affects multiple package configurations due to potential methanol contamination. Consumers should stop using the product immediately and contact the company for guidance.

Acuity Specialty Products
cGMP deviations:
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HIGHFDA FOOD

Wegmans Cheesecake Recalled Due to Undeclared Pecan Hazard

Wegmans recalled 2,216 units of Ultimate Plain Cheesecake on September 29, 2025. The product contains undeclared pecans, posing a serious allergy risk. Customers in Pennsylvania and Virginia should not consume this item.

Eli's Cheesecake
undeclared pecan
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HIGHFDA DRUG

AFCO Hand Sanitizer Recalled Due to Methanol Risk

AFCO recalled hand sanitizer on September 29, 2025, due to a risk of methanol contamination. The company failed to conduct required testing on incoming alcohol components. Consumers should stop using the product immediately.

AFCO
cGMP deviations:
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HIGHFDA FOOD

Vicky IT Recalls Bona Fish Due to Botulism Risk

Vicky IT Inc. recalled 10 lbs of Bona Fish on September 27, 2025. The product poses a high risk of contamination with Clostridia botulinum, mold, and filth. Consumers should not eat the fish and seek refunds immediately.

Vicky IT
Fish is
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