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.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
January 14, 2026
Status
ACTIVE
Severity
7/10

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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.

  1. Recall announced

    January 14, 2026

  2. Reported by FDA DRUG

    February 18, 2026

  3. RecallRadar source check

    February 25, 2026

  4. 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

  1. Check the lot numbers on the blister card packaging: 1027932 and 1028360.
  2. Verify the expiration dates: 06/30/2027 and 08/31/2027.
  3. 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

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lots #: 1027932
Exp Date 06/30/2027
1028360
Exp Date 08/31/2027
UPC Codes
68084-354
68084-968
68084-975
+9 more
Affected States
ALL
Report Date
February 18, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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