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

2,247 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 DRUG

Chlorpromazine Hydrochloride Tablets Recalled Over Contamination Risk

American Health Packaging recalled 1,062 cartons of Chlorpromazine Hydrochloride Tablets on August 27, 2025. The recall stems from the detection of a micro-organism in auxiliary packaging materials. No micro-organism was found on the tablets themselves, but consumers should stop using the product immediately.

CHLORPROMAZINE HYDROCHLORIDE
Presence of
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HIGHFDA FOOD

Middlefield Cheese Co-op Recalls Shredded Cheese for Listeria Risk

Middlefield Original Cheese Cooperative recalled 364 cases of shredded mozzarella/provolone cheese on August 27, 2025, due to potential Listeria contamination. This recall affects 7,455 pounds of cheese distributed in Ohio, Pennsylvania, Wisconsin, and Texas. Consumers should not eat the product and seek refunds or replacements immediately.

Middlefield Original Cheese Cooperative
Potential contamination
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HIGHFDA FOOD

Middlefield Original Cheese Co-op Recalls Organic Gouda Over Listeria Risk

Middlefield Original Cheese Co-op recalled 364 cases of Organic Gouda Cheese on August 27, 2025. The recall follows potential contamination with Listeria monocytogenes, which can cause serious illness. Consumers should not eat the cheese and seek refunds or replacements.

Middlefield Original Cheese Cooperative
Potential contamination
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HIGHFDA DEVICE

Vision RT Recalls AlignRT InBore System Over Laser Omission Hazard

Vision RT recalled 56 AlignRT InBore systems on August 27, 2025, due to missing safety information in the Instructions for Use. The omission pertains to the identification and characteristics of the system's Class 1 lasers as required by federal regulations. Users must stop using the device immediately and follow manufacturer instructions.

Vision RT
Vision RT
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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 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 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 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 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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