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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Oxycodone Hydrochloride Tablets are prescription medications used to manage pain. They are typically prescribed for moderate to severe pain relief.
Defective seals on the packaging can lead to tablets falling out, which increases the risk of misuse, accidental ingestion, or reduced effectiveness of the medication.
This recall is not part of a broader industry pattern.
Consumers may face inconvenience and health risks due to the potential misuse or accidental ingestion of fallen tablets.
The lot numbers and expiration dates are usually found on the outer packaging of the blister card or on the blister itself.
Refund processing may take 4-6 weeks after returning the recalled product.
Keep receipts, photos of the product, and any correspondence related to the recall as documentation.
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.
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