Quick Facts at a Glance
- Recall Date
- January 14, 2026
- Hazard Level
- HIGH
- Brands
- OXYCODONE HYDROCHLORIDE, American Health Packaging
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- OXYCODONE HYDROCHLORIDE, American Health Packaging
- Product type
- Oxycodone Hydrochloride Tablets
- Model numbers
- Lots #: 1027932, Exp Date 06/30/2027, 1028360, Exp Date 08/31/2027
- UPC codes
- 68084-354, 68084-968, 68084-975, 68084-983, 68084-354-11, 68084-354-01, 68084-968-11, 68084-968-01 +4 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 14, 2026
Reported by FDA DRUG
February 18, 2026
RecallRadar source check
February 25, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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.
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Amerisource Health Services LLC or your healthcare provider for guidance. Notification method: Letter
About This Product
Oxycodone Hydrochloride Tablets are prescription medications used to manage pain. They are typically prescribed for moderate to severe pain relief.
Why This Is Dangerous
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.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers may face inconvenience and health risks due to the potential misuse or accidental ingestion of fallen tablets.
Practical Guidance
How to identify if yours is affected
- Check the lot numbers on the blister card packaging: 1027932 and 1028360.
- Verify the expiration dates: 06/30/2027 and 08/31/2027.
- If your product matches these details, it is part of the recall.
Where to find product info
The lot numbers and expiration dates are usually found on the outer packaging of the blister card or on the blister itself.
What timeline to expect
Refund processing may take 4-6 weeks after returning the recalled product.
If the manufacturer is unresponsive
- Follow up with the retailer where the product was purchased.
- Contact Amerisource Health Services LLC again for further assistance.
How to prevent similar issues
- Always inspect medication packaging for integrity before use.
- Only purchase medications from reputable pharmacies.
Documentation advice
Keep receipts, photos of the product, and any correspondence related to the recall as documentation.
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Product Details
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.
Key Facts
- Recall date: January 14, 2026
- Quantity recalled: 31,676 packages
- Distribution: Nationwide in the USA
- Hazard classification: Class II
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Safety Guide
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