American Health Packaging Recalls

9 recalls found for American Health Packaging. Check if any of your products are affected.

HIGHFDA DRUG

KVK-Tech Inc. Recalls Oxycodone Hydrochloride Tablets Over Seal Defects

KVK-Tech Inc. recalled 31,676 packages of Oxycodone Hydrochloride Tablets on January 14, 2026. Defective seals may cause tablets to fall out, posing a health risk. Customers should stop using the product immediately and seek guidance from healthcare providers.

OXYCODONE HYDROCHLORIDE
Defective container:
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HIGHFDA DRUG

American Health Packaging Recalls Sucralfate Tablets Over Quality Concerns

American Health Packaging recalled 27,868 blister packs of Sucralfate Tablets on October 9, 2025. The company filed for Chapter 11 bankruptcy, impairing its ability to monitor product quality. Consumers should stop using the product immediately and seek guidance from healthcare providers.

SUCRALFATE
CGMP Deviations:
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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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