All Product Recalls

Browse through 1,540 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

HIGHFDA DEVICE

American Contract Systems Recalls Medical Kits Over Safety Risk

American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. These kits failed to meet safety standards due to improper sterilization processes. The recall affects multiple states, including South Dakota and Iowa.

American Contract Systems
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HIGHFDA FOOD

Pacific Coast Producers Recalls Canned Pears Over Lead Contamination

Pacific Coast Producers recalled 1,836 cases of canned pears on September 4, 2025, due to potential lead contamination. The affected product includes pears in pear juice concentrate sold in 15-ounce cans. Consumers should not consume the product and seek refunds immediately.

Pacific Coast Producers
Potential contamination
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HIGHFDA DEVICE

American Contract Systems Biopsy Tray Recalled Over Sterilization Issues

American Contract Systems recalled 32,433 Basic Biopsy Trays on September 4, 2025. The recall resulted from products being re-gassed after a sterilization failure. The company cannot confirm the safety or effectiveness of these devices after multiple sterilization cycles.

American Contract Systems
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HIGHFDA FOOD

Wegmans Recalls Halved Pears Due to Lead Contamination Risk

Wegmans Food Markets recalled 102 cases of halved pears in pear juice on September 4, 2025. The recall follows concerns of potential lead contamination. Consumers should not consume the product and seek refunds.

Pacific Coast Producers
Potential contamination
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HIGHFDA DEVICE

American Contract Systems Recalls Medical Kits Over Sterilization Issues

American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall follows the identification of products that were re-gassed after sterilization failures. The safety and effectiveness of these products cannot be confirmed due to multiple sterilization cycles.

American Contract Systems
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HIGHFDA DEVICE

American Contract Systems Recalls Medical Kits Over Sterilization Risk

American Contract Systems recalled 32,433 medical convenience kits after multiple sterilization cycles compromised product safety. The recall, announced on September 4, 2025, stems from nonconformance during Ethylene Oxide gas sterilization. Affected products include kits used for cataract and eye procedures.

American Contract Systems
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HIGHFDA FOOD

Good and Gather Burrito Bowl Blend Recalled for Undeclared Shrimp

Good and Gather recalled 57,240 bags of Southwest-Style Burrito Bowl Blend on September 4, 2025. The product may contain undeclared shrimp, posing a serious risk to those with shellfish allergies. Consumers should not consume the product and contact ONE FROZEN for refunds or replacements.

ONE FROZEN
Product may
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HIGHFDA FOOD

Wegmans Recalls Fruit Cocktail Due to Lead Contamination Risk

Wegmans Food Markets recalled 609 cases of Fruit Cocktail on September 4, 2025, due to potential lead contamination. The affected product includes diced peaches and pears, distributed across multiple states. Consumers should not consume the recalled product and seek a refund or replacement.

Pacific Coast Producers
Potential contamination
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HIGHFDA DEVICE

American Contract Systems Recalls Medical Kits Over Sterilization Issues

American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall follows issues with multiple sterilization cycles that compromise product safety. Patients and healthcare providers should stop using these devices immediately.

American Contract Systems
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HIGHFDA DEVICE

Philips Medical Imaging System Recalled for Motorized Movement Risk

Philips Medical Systems Nederland B.V. recalled 46 imaging systems on September 3, 2025. Deterioration of internal components may lead to loss of motorized movements. Healthcare providers must stop using the systems immediately and follow recall instructions.

Philips Medical Systems Nederland B.V.
Systems may
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HIGHFDA DRUG

Zydus Lifesciences Recalls Chlorpromazine Tablets Due to Hazard

Zydus Lifesciences recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The tablets contain N-Nitroso Desmethyl Chlorpromazine above safe intake levels. Consumers must stop using the product immediately and consult healthcare providers.

Zydus Lifesciences
CGMP Deviations:
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HIGHFDA FOOD

Endico Mixed Vegetables Recalled Due to Listeria Contamination

Endico Potatoes Inc recalled 280 cases of mixed vegetables on September 3, 2025. The frozen product may be contaminated with Listeria monocytogenes. It was distributed in New York, New Jersey, Connecticut, Florida, Pennsylvania, Maryland, and Washington, D.C.

Endico Potatoes
Product may
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HIGHFDA DRUG

Zydus Lifesciences Recalls Chlorpromazine Tablets Over Chemical Hazard

Zydus Lifesciences Ltd. recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects products with NDC 16714-050-01 due to high levels of a chemical impurity. Consumers should stop using the tablets immediately and contact healthcare providers.

Zydus Lifesciences
CGMP Deviations:
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HIGHFDA DEVICE

Philips Medical Systems Recalls Operating Room Tables Due to Hazard

Philips Medical Systems Nederland B.V. recalled two operating room tables on September 3, 2025. The recall affects models 722022 and 722033 due to potential system failures. The malfunction can inhibit motorized movements, posing a risk to patients and healthcare providers.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Systems may
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HIGHFDA DRUG

Zydus Pharmaceuticals Recalls Chlorpromazine Tablets Over Contamination

Zydus Pharmaceuticals recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects a specific lot due to contamination with N-Nitroso Desmethyl Chlorpromazine. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Chlorpromazine Hydrochloride
CGMP Deviations:
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