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.

Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

American Health Packaging BuPROPion HCl Tablets Recalled for Impurities

Agency Publication Date: February 16, 2023
Share:
Sign in to monitor this recall

Summary

Amerisource Health Services LLC has recalled 1,416 cartons of American Health Packaging BuPROPion Hydrochloride Tablets (bupropion hydrochloride) because they failed quality tests for impurities and degradation. The recalled medication consists of 75 mg tablets packaged in cartons of 100 (10 x 10 blister packs). No injuries or illnesses have been reported to date, but consumers are advised to stop using the affected tablets immediately and consult their healthcare provider.

Risk

The tablets failed to meet safety specifications for impurities and chemical degradation, which can reduce the medication's effectiveness or expose patients to unexpected byproducts. While no incidents are reported, using degraded medication poses a risk to patients relying on the drug for treatment.

What You Should Do

  1. This recall affects American Health Packaging BuPROPion Hydrochloride Tablets, USP 75 mg, sold in cartons of 100 (10 x 10 blister packs) with lot number 1003837 and expiration date 01/31/2023.
  2. Identify the product by checking the carton for NDC 60687-340-01 or the individual blister packs for NDC 60687-340-11.
  3. 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 Amerisource Health Services LLC for further instructions.
  4. 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:

๐Ÿ’ฐOption 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
๐Ÿ—‘๏ธ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: BuPROPion Hydrochloride Tablets, USP 75 mg, 100 Tablets (10 x 10) per cartonby American Health Packaging
Variants: 75 mg, Tablet
Lot Numbers:
1003837 (Exp 01/31/2023)
NDC:
60687-340-01
60687-340-11

Distributed by American Health Packaging, Columbus, Ohio.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91609
Status: Resolved
Manufacturer: Amerisource Health Services LLC
Sold By: American Health Packaging
Manufactured In: United States
Units Affected: 1,416 cartons
Distributed To: Nationwide

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 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.