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

2,324 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

Kosher First Recalls Herring Due to Undeclared FD&C Red #40

Kosher First recalled 283 units of Shloimy's Heimishe Matjes Herring on November 10, 2025, due to undeclared FD&C Red #40. The recall affects products distributed in New York and poses a high risk of allergic reactions. Consumers should not consume the product and seek refunds or replacements.

Kosher First
Undeclared FD&C
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HIGHFDA DEVICE

Draeger Recalls Airway Connector Due to Cracking Hazard

Draeger recalled 2,050 units of the ErgoStar CM 60 airway connector on November 10, 2025. The recall follows multiple reports of cracks in the device, posing a risk to mechanically ventilated patients. Healthcare providers and patients should stop using the connector immediately.

Draeger
Multiple complaints
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HIGHFDA DEVICE

Draeger Recalls Airway Connector Due to Cracks in Hose

Draeger recalled 191,470 units of the ErgoStar CM 45 airway connector on November 10, 2025. Users reported cracks in the hose of specific catheter mounts, posing a high risk to patients. The recall affects healthcare facilities worldwide, including multiple U.S. states.

Draeger
Multiple complaints
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HIGHFDA DEVICE

Draeger Recalls Airway Connector Over Cracking Hazard

Draeger recalled 14,420 units of its ErgoStar CM 40 airway connector on November 10, 2025, due to cracks forming in the hose. The recall affects multiple states in the U.S. and several countries worldwide.

Draeger
Multiple complaints
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HIGHFDA DEVICE

Waldemar Link Recalls Knee Fusion Nail Due to Assembly Error

Waldemar Link GmbH & Co. KG recalled 18 units of the Endo Model Knee Fusion Nail SK on November 10, 2025. The device features a preassembled locking screw incorrectly inserted, posing a high risk of failure. Affected units were distributed in Alabama, Georgia, and Texas.

Waldemar Link GmbH & Co. KG
The device
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HIGHFDA DEVICE

Draeger Recalls Airway Connector Over Cracking Hazard

Draeger recalled 118,850 airway connectors on November 10, 2025, due to cracking hazards. This recall affects multiple countries, including the United States and Australia. The device poses a serious risk to mechanically ventilated patients.

Draeger
Multiple complaints
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HIGHFDA DEVICE

Beckman Coulter Recalls Diluent Due to Elevated Platelet Counts

Beckman Coulter recalled 76,098 units of COULTER DxH Diluent on November 10, 2025. The recall affects specific lots contributing to elevated platelet background counts in analyzers. Healthcare providers and patients must stop using this product immediately.

Beckman Coulter
Due to
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HIGHNHTSA

Chrysler Recalls 2025 Jeep Wagoneer Over Detachable Trim Hazard

Chrysler is recalling certain 2022-2025 Jeep Wagoneer and Grand Wagoneer vehicles. Improperly installed trim on the driver and passenger doors may detach, creating a road hazard. The recall affects an unknown number of vehicles manufactured through 2025.

Chrysler
Detached trim
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HIGHNHTSA

Toyota Camry Recalled for Electrical System Failure Risk

Toyota recalled the 2025 Camry due to a software issue that affects the instrument panel. The malfunction can obscure critical driving information, increasing crash risk. Notification letters will be sent to owners by October 27, 2025.

Toyota
An instrument
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HIGHNHTSA

Ford Recalls 2025 Explorer Due to Fuel Leak Risk

Ford Motor Company recalled the 2025 Explorer on November 8, 2025. The recall affects vehicles with fuel injectors potentially lacking O-ring support discs. A fuel leak could increase the risk of fire.

Ford Motor Company
A fuel
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HIGHFDA FOOD

ByHeart Infant Formula Recalled Due to Botulism Risk

ByHeart announced a recall of over 6.9 million units of its infant formula on November 8, 2025, due to contamination with Clostridium botulinum. The recall affects both cans and single-serve packets sold nationwide. Parents are urged to stop using the affected products immediately to prevent serious health risks.

ByHeart
Contaminated with
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HIGHNHTSA

Toyota Recalls 2025 Camry Hybrid Over Inaccurate Load Labels

Gulf States Toyota is recalling 2025 Camry Hybrid vehicles due to incorrect load capacity labels. The recall affects an unspecified number of vehicles sold since 2023. Faulty labels may lead to overloading and increase crash risk.

Gulf States Toyota
A vehicle
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HIGHFDA DRUG

Actavis Recalls Testosterone Gel Due to Leakage Risk

Actavis Laboratories recalled 15,944 cartons of Testosterone Gel on November 7, 2025. The recall follows a defect in the side-seal of the containers, which may allow product leakage. Consumers must stop using the product immediately and contact their healthcare providers for guidance.

TESTOSTERONE
Defective Container
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