All Product Recalls

Browse through 474 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

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
Read more
Recalled Nimbus Lock Carabiners
HIGH
CPSC

C.A.M.P. Recalls Nimbus Lock Carabiners Due to Fall Risk

C.A.M.P. recalled Nimbus Lock Carabiners on August 28, 2025, after discovering a defect that can prevent the gate from closing. This poses a significant risk of serious injury or death from falls. The recall affects carabiners sold in multiple colors and batch numbers between October 2023 and June 2025.

Nimbus
The carabiner's
Read more
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
Read more
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
Read more
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
Read more
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
Read more
Recalled DT Swiss Carbon Fiber Road Wheels
MEDIUM
CPSC

DT Swiss Recalls Carbon Wheels Due to Crash Hazard

DT Swiss recalled carbon fiber road wheels due to a structural defect that may cause crashes. The recall affects wheels with model codes ERC 35mm/45mm, CRC 35mm/45mm, HEC 35mm/45mm, and ARC 50mm/55mm/65mm. Consumers should stop using these wheels immediately and contact the company for a replacement.

DT Swiss
A defect
Read more
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
Read more
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
Read more
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
Read more
HIGHFDA FOOD

Middlefield Original Cheese Co-op Recalls Shredded Mozzarella Cheese

Middlefield Original Cheese Cooperative recalled 7,455 pounds of shredded mozzarella cheese on August 27, 2025. The product may contain Listeria monocytogenes, which can cause serious illness. Consumers should not consume the cheese and seek refunds or replacements.

Middlefield Original Cheese Cooperative
Potential contamination
Read more
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
Read more
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
Read more
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
Read more
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
Read more
Advertisement