Medications & Supplements/Prescription Drugs

Oxycodone Hydrochloride Tablets Recalled for Defective Blister Seals

Agency Publication Date: February 10, 2026

Summary

Amerisource Health Services LLC is recalling 31,676 packages of Oxycodone Hydrochloride Tablets (5 mg) because of defective blister card seals. The seals on the individual tablet cavities may be weak or non-existent, which can cause the tablets to fall out of their protective packaging. This recall affects 100-count cartons (containing 10 blister cards of 10 tablets each) that were distributed nationwide.

Risk

Defective seals can lead to tablets falling out of their blister cavities, potentially resulting in the loss of medication, accidental ingestion by unauthorized users, or reduced integrity of the drug product. No injuries or specific medical incidents were reported in the recall notice.

What You Should Do

Check your medication packaging for Oxycodone Hydrochloride Tablets, USP (CII), 5 mg in 100-count cartons (10 x 10 blister cards).
Locate the lot number and expiration date on the carton or blister card. Affected products include lot 1027932 (Exp 06/30/2027) and lot 1028360 (Exp 08/31/2027).
Check the NDC numbers on the packaging: the carton NDC is 68084-354-01 and the blister NDC is 68084-354-11.
If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

Option 1: Full Refund

How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund

Option 2: Dispose of Product

How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Oxycodone Hydrochloride Tablets, USP (CII), 5 mg (100-count)

Variants: 5 mg, Tablet

Lot Numbers:

1027932 (Exp 06/30/2027)

1028360 (Exp 08/31/2027)

NDC:

68084-354-01

68084-354-11

10702-018

Distributed by American Health Packaging; Product contained in package is from KVK-Tech Inc.

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 98308

Status: Active

Manufacturer: Amerisource Health Services LLC

Sold By: Pharmacies

Manufactured In: United States

Units Affected: 31,676 packages

Distributed To: Nationwide

Agency Last Updated: April 22, 2026

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.

Summary

What You Should Do

Check your medication packaging for Oxycodone Hydrochloride Tablets, USP (CII), 5 mg in 100-count cartons (10 x 10 blister cards).

Locate the lot number and expiration date on the carton or blister card. Affected products include lot 1027932 (Exp 06/30/2027) and lot 1028360 (Exp 08/31/2027).

Check the NDC numbers on the packaging: the carton NDC is 68084-354-01 and the blister NDC is 68084-354-11.

If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.

Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions regarding this recall.