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.
Defective container: Multiple customer complaints received for card seal defects observed on the subject lots. Customers reported card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
Consumers and healthcare providers should stop using this product immediately. Contact Amerisource Health Services LLC or your healthcare provider for guidance. Notification method: Letter
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The recall involves Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, packaged in 100-count blister cards. This product is identified by NDC # 10702-018, distributed by American Health Packaging.
The recall stems from reports of defective container seals. Weak or non-existent seals can result in tablets falling out, increasing the risk of misuse or accidental ingestion.
Stop using the recalled product immediately. Contact Amerisource Health Services LLC or your healthcare provider for further direction.
For assistance, call Amerisource Health Services LLC at 1-800-XXXX-XXXX. More details are available on the FDA website.
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