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

456 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
Recalled CT-ENERGY Lithium Coin Battery Charger with Rechargeable 2032 Batteries
HIGH
CPSC

CT-ENERGY Battery Chargers Recalled Over Serious Injury Risk

CT-ENERGY recalled Lithium Coin Battery Chargers on August 28, 2025. The chargers can expose children to easily accessible lithium batteries, posing a risk of serious injury or death from ingestion. Consumers should stop using the product immediately and seek refunds.

CT-ENERGY
The recalled
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HIGHFDA DRUG

Granules Pharmaceuticals Recalls Dextroamphetamine Capsules for Impurities

Granules Pharmaceuticals Inc. recalled 11,895 bottles of extended-release capsules on August 28, 2025. The capsules failed impurities and degradation specifications. Consumers should stop using the product immediately, as it could pose health risks.

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate
Failed Impurities/Degradation
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HIGHFDA DRUG

Granules Pharmaceuticals Recalls Amphetamine Capsules for Degradation Issues

Granules Pharmaceuticals Inc. recalled 3,384 bottles of amphetamine capsules on August 28, 2025. The recall follows a failure to meet impurities and degradation specifications. Consumers should stop using this product immediately and consult healthcare providers.

Granules Pharmaceuticals Inc.
Failed Impurities/Degradation
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HIGHFDA DRUG

Granules Pharmaceuticals Recalls Amphetamine Capsules Over Impurity Risks

Granules Pharmaceuticals recalled 11,928 bottles of amphetamine capsules on August 28, 2025. The recall follows failure to meet impurities and degradation specifications. Consumers should stop using the product immediately and contact their healthcare providers.

Granules Pharmaceuticals
Failed Impurities/Degradation
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HIGHFDA DRUG

Ascend Laboratories Recalls Aripiprazole Tablets Due to Potency Risk

Ascend Laboratories, LLC recalled 2,256 bottles of Aripiprazole Tablets on August 28, 2025. The recall followed reports that the drug may be superpotent, posing serious health risks. Consumers should stop using the product immediately and consult healthcare providers.

ARIPIPRAZOLE
Superpotent drug
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HIGHFDA DRUG

Granules Pharmaceuticals Recalls Dextroamphetamine Capsules Over Contamination Risk

Granules Pharmaceuticals Inc. recalled 9,917 bottles of Dextroamphetamine extended-release capsules on August 28, 2025. The product failed impurities and degradation specifications, posing potential health risks. Consumers should stop using the capsules immediately and consult healthcare providers for guidance.

Granules Pharmaceuticals
Failed Impurities/Degradation
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HIGHFDA DRUG

Granules Pharmaceuticals Recalls Dextroamphetamine Capsules Over Impurity Concerns

Granules Pharmaceuticals Inc. recalled 11,909 bottles of Dextroamphetamine extended-release capsules on August 28, 2025. The recall stems from failure to meet impurities and degradation specifications. Healthcare providers and consumers must stop using the product immediately.

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate
Failed Impurities/Degradation
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HIGHFDA FOOD

Middlefield Cheese Recalled Due to Listeria Contamination Risk

Middlefield Original Cheese Cooperative recalled 364 cases of Swiss cheese on August 27, 2025. The recall stems from potential contamination with Listeria monocytogenes. Consumers should not consume the product and seek refunds immediately.

Middlefield Original Cheese Cooperative
Potential contamination
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HIGHFDA FOOD

Middlefield Cheese Co-op Issues Recall for Smoked Cheddar Due to Listeria Risk

Middlefield Original Cheese Cooperative recalled 364.125 cases of Smoked Cheddar on August 27, 2025. The cheese may be contaminated with Listeria monocytogenes, posing a high health risk. Consumers in Ohio, Pennsylvania, Wisconsin, and Texas should not consume the product.

Middlefield Original Cheese Cooperative
Potential contamination
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HIGHFDA FOOD

Middlefield Cheese Coop Recalls Cheddar Cheese for Listeria Risk

Middlefield Original Cheese Cooperative recalled 364 cases of cheddar cheese on August 27, 2025. The products may contain Listeria monocytogenes, a harmful bacteria. Consumers should avoid eating the cheese and seek refunds or replacements.

Middlefield Original Cheese Cooperative
Potential contamination
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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 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

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 DRUG

American Health Packaging Recalls Chlorpromazine Tablets Over Contamination Risk

American Health Packaging recalled 1,757 cartons of Chlorpromazine Hydrochloride Tablets on August 27, 2025. The recall stems from the detection of a microorganism in packaging materials, though no contamination was found on the tablets themselves. Consumers should stop using the product immediately and contact healthcare providers for guidance.

Chlorpromazine Hydrochloride
Presence of
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HIGHFDA DRUG

Unichem Pharmaceuticals Recalls Cyclobenzaprine Tablets Due to Labeling Error

Unichem Pharmaceuticals recalled 230 bottles of Cyclobenzaprine Hydrochloride Tablets on August 27, 2025. The recall stems from a labeling mix-up with Meloxicam tablets, which could lead to serious health risks. Consumers should stop using the product immediately and contact their healthcare provider.

CYCLOBENZAPRINE HYDROCHLORIDE
Labeling: Label
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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 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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