These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.

High Risk Recalls

621 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.

What to do if you own a recalled product:

  1. Stop using the product immediately
  2. Keep the product away from children
  3. Follow the remedy instructions provided
  4. Contact the manufacturer for a refund or replacement
HIGHFDA FOOD

Organicare Nature's Science Recalls FemiClear Supplement Over E. Coli Risk

Organicare Nature's Science recalled 15,075 bottles of FemiClear Daily Bladder Strength Dietary Supplement on September 4, 2025. The recall stems from microbial contamination with E. coli O7:K1 and E. coli 1303. Consumers should not consume the product and seek refunds immediately.

Organicare Nature's Science
Microbial contamination
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HIGHFDA DEVICE

Philips Medical Systems Recalls Imaging Devices Due to Hazard

Philips Medical Systems recalled 286 Allura Xper FD10/10 imaging systems on September 3, 2025. The recall affects models 722011, 722027, and 722005 due to potential failure of internal components. This malfunction could inhibit motorized movements, posing risks to patient safety.

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

Philips Medical Systems Recalls X-ray Imaging Systems Due to Malfunction Risk

Philips Medical Systems Netherlands B.V. recalled 1,117 X-ray imaging systems on September 3, 2025. The recall affects product codes 722010, 722026, and 722003 due to potential internal component deterioration. This issue may render motorized movements inoperable, posing a risk to patient care.

Philips Medical Systems Netherlands B.V.
Systems may
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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 Recalls Chlorpromazine Hydrochloride Tablets Over Contamination Hazard

Zydus Lifesciences Ltd. recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects 10 mg tablets sold nationwide due to contamination with N-Nitroso Desmethyl Chlorpromazine. Consumers should 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 DEVICE

Philips Medical Systems Recalls Radiology Imaging Systems for Safety Issues

Philips Medical Systems Nederland B.V. recalled 98 radiology imaging systems on September 3, 2025. The recall stems from internal component deterioration that may hinder motorized movements. Patients and healthcare providers must stop using the devices immediately.

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

Philips Medical Systems Recalls Operating Table Due to Hazard

Philips Medical Systems Nederland B.V. recalled the Allura Xper FD20/15 OR Table on September 3, 2025. The recall affects one unit distributed worldwide, including the U.S. Systems may not perform as intended due to internal component deterioration.

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

Philips Medical Systems Recalls OR Tables Over Motorized Movement Failure

Philips Medical Systems Nederland B.V. recalled 174 OR tables on September 3, 2025. The recall affects models 722023, 722035, and 722015 due to potential failure of motorized movements. Users must stop using these devices immediately to prevent operational issues.

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

Endico Frozen Peas and Carrots Recalled Due to Listeria Risk

Endico Potatoes Inc recalled 335 cases of frozen peas and carrots on September 3, 2025. The products may contain Listeria monocytogenes, a bacteria that can cause serious illness. The affected items were distributed in several states including New York and Florida.

Endico Potatoes
Product may
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HIGHFDA DEVICE

Philips Medical Systems Recalls Imaging Systems Over Malfunction Risk

Philips Medical Systems Nederland B.V. recalled 268 Allura Xper FD20 Biplane systems on September 3, 2025. The recall affects units distributed globally due to potential failures in internal components. If malfunction occurs, motorized movements will be disabled, posing risks to operational efficiency.

Philips Medical Systems
Systems may
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HIGHFDA DRUG

Zydus Lifesciences Recalls Chlorpromazine Tablets Over Contaminant Hazard

Zydus Lifesciences recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects tablets with NDC 16714-051-01 due to N-Nitroso Desmethyl Chlorpromazine exceeding acceptable limits. Consumers should stop using the product immediately and consult healthcare providers.

Zydus Lifesciences
CGMP Deviations:
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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 DEVICE

Philips Medical Systems Recalls Operating Room Table Over Hazard

Philips Medical Systems Netherlands B.V. recalled three Allura Xper FD20/20 OR Tables on September 3, 2025. The recall addresses potential failures in internal components that could impede motorized functions. Users must stop using the device immediately and follow recall instructions.

Philips Medical Systems Netherlands B.V.
Systems may
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HIGHFDA DEVICE

Philips Medical Systems Recalls Imaging System Over Malfunction Risk

Philips Medical Systems Nederland B.V. recalled 75 Allura Xper FD20/20 imaging systems on September 3, 2025. The recall affects systems due to internal component deterioration, which can hinder motorized movements. All users must stop using the device immediately and follow manufacturer instructions for safe handling.

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

Philips Medical Systems Recalls X-Ray Imaging Systems Due to Hazard

Philips Medical Systems Nederland B.V. recalled 45 Allura Xper FD20/10 imaging systems on September 3, 2025. The systems may fail due to internal component deterioration, posing a high risk to users. Affected units include 11 in the U.S. and 34 internationally.

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

Zydus Lifesciences Recalls Chlorpromazine Tablets Due to Contamination

Zydus Lifesciences Ltd. recalled Chlorpromazine Hydrochloride Tablets on September 3, 2025. The recall affects tablets containing N-Nitroso Desmethyl Chlorpromazine above safe limits. Consumers should stop using the product immediately and consult healthcare providers.

Zydus Lifesciences
CGMP Deviations:
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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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