All Product Recalls

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

HIGHFDA FOOD

Middlefield Cheese Recalled Due to Listeria Contamination Risk

Middlefield Original Cheese Cooperative recalled 364 cases of Pepper Jack Cheese on August 27, 2025. The recall follows potential contamination with Listeria monocytogenes. Consumers should not eat the product and seek refunds or replacements.

Middlefield Original Cheese Cooperative
Potential contamination
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HIGHFDA DRUG

Neuroquell Recall Issued Over cGMP Violations

Claire Ellen Products recalled 72 containers of Neuroquell and Neuroquell Plus on August 27, 2025. The recall follows violations of current Good Manufacturing Practices (cGMP). Consumers must stop using the products immediately and consult healthcare providers for guidance.

Claire Ellen Products
cGMP violations
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HIGHFDA DRUG

Zydus Pharmaceuticals Recalls Succinylcholine Chloride Injection Due to Hazards

Zydus Pharmaceuticals recalled 270,125 vials of Succinylcholine Chloride Injection on August 27, 2025. The recall follows failed impurity tests indicating unknown degradation issues. Consumers and healthcare providers must stop using the product immediately and seek guidance.

Succinylcholine Chloride
Failed Impurities/Degradation
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HIGHFDA DRUG

B. Braun Medical Recalls Sterile Water for Injection Due to Sterility Risk

B. Braun Medical Inc. recalled 26,316 bags of Sterile Water for Injection on August 26, 2025. The recall affects the 3000 mL product due to potential fluid leakage from a misaligned port. Consumers should stop using the product immediately and seek guidance from healthcare providers.

B. Braun Medical Inc.
Lack of
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HIGHFDA FOOD

Extract Labs Recalls Gummies Due to Peanut Protein Risk

Extract Labs recalled 2,180 bottles of sugar-free mixed berry gummies on August 26, 2025. The recall stems from potential peanut protein cross-contact, posing a risk to consumers with allergies. The gummies contain 10mg of CBD and 10mg of D9 THC per serving.

Extract Labs
Potential peanut
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HIGHFDA FOOD

Extract Labs Recalls Elderberry Gummies Over Peanut Protein Risk

Extract Labs recalled 19,720 Elderberry gummies on August 26, 2025 due to potential peanut protein cross-contact. The gummies, containing 20mg CBD and 20mg D9 THC each, were shipped unlabeled in bulk packaging. Consumers should not consume these products and seek refunds or replacements.

Extract Labs
Potential peanut
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HIGHFDA DRUG

B. Braun Medical Issues Recall for Sodium Chloride Irrigation Solution

B. Braun Medical Inc. recalled 16,228 bags of Sodium Chloride Irrigation Solution on August 26, 2025. The recall stems from a lack of assurance of sterility, posing a high risk of contamination. Consumers and healthcare providers should stop using the product immediately and seek guidance from B. Braun or their healthcare provider.

B. Braun Medical Inc.
Lack of
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HIGHFDA FOOD

Extract Labs Recalls Mai Tai Gummies Over Peanut Protein Risk

Extract Labs recalled 19,750 gummies on August 26, 2025, due to potential peanut protein cross-contact. The products, which contain 20mg of CBD and 20mg of D9 THC per gummy, lack proper labeling. Consumers should not consume these gummies and should contact the company for refunds or replacements.

Extract Labs
Potential peanut
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HIGHFDA DEVICE

W L Gore & Associates Recalls Vascular Grafts Over Delamination Risk

W L Gore & Associates recalled over 52,000 vascular grafts on August 26, 2025, due to reports of delamination. The defect can lead to severe complications such as bleeding or cannulation difficulties. Affected products include multiple model numbers, which were distributed across the United States and internationally.

W L Gore & Associates
Reports of
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HIGHFDA DRUG

AvKare Recalls Chlorpromazine Tablets Due to Foreign Substance

AvKare recalled 2,003 cartons of Chlorpromazine Hydrochloride Tablets on August 25, 2025. The recall stems from the presence of a foreign substance in the medication. Consumers should stop using the product immediately and seek guidance from healthcare providers.

CHLORPROMAZINE HYDROCHLORIDE
Presence of
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HIGHFDA DEVICE

CooperVision Recalls Contact Lenses Due to Sterilization Error

CooperVision recalled 90 units of Voyant 1-Day Premium Toric contact lenses on August 22, 2025. The recall affects one lot manufactured with an invalid sterilization cycle. Consumers should stop using the product immediately and follow recall instructions.

CooperVision
One lot
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