Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Low RiskFDA Drug
Medications & Supplements/Prescription Drugs

American Health Packaging: Lamivudine Tablets Recalled for Incorrect Package Insert Information

Agency Publication Date: September 6, 2019
Share:
Sign in to monitor this recall

Summary

American Health Packaging has recalled 60 cartons of Lamivudine Tablets (150 mg), which is the generic version of Epivir used to treat HIV-1 and Hepatitis B. The recall was issued because the package insert incorrectly describes the tablets' appearance in the "Dosage Forms and Strengths" section. This labeling error could lead to confusion about whether the patient is taking the correct medication or dosage. The affected products were distributed nationwide in unit-dose blister packs. Consumers should contact their doctor or pharmacist to confirm they have the correct medication and return any products from the affected lots for a refund.

Risk

An incorrect physical description of the tablet in the package insert can cause patients or healthcare providers to misidentify the medication or its strength. This increases the risk of medication errors, potentially leading to improper dosing or missed treatments.

What You Should Do

  1. Check your medication packaging for Lamivudine Tablets, USP, 150 mg, in 30-count Unit Dose Blister Cartons with NDC 60687-362-21 or individual dose NDC 60687-362-11.
  2. Identify if your product belongs to lot 186509 or lot 186982, both with an expiration date of 6/30/2021.
  3. If you have an affected product, contact your healthcare provider or pharmacist immediately to verify the medication and ensure your treatment is not interrupted.
  4. Return any unused product from these specific lots to the pharmacy where it was purchased for a refund.
  5. Contact American Health Packaging at 2550 John Glenn Ave Ste A, Columbus, Ohio, 43217-1188 for further instructions regarding this recall.
  6. For additional questions, call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Refund and medical guidance

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Lamivudine Tablets, USP, 150 mg, 30 (3x10) count Unit Dose Blisters Carton
Model:
NDC 60687-362-21
NDC 60687-362-11
Lot Numbers:
186509 (Exp 6/30/2021)
186982 (Exp 6/30/2021)
Date Ranges: 6/30/2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 83672
Status: Resolved
Manufacturer: American Health Packaging
Manufactured In: United States
Units Affected: 60 cartons
Distributed To: Nationwide

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 ยท 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.