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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.

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Medium RiskFDA Drug
Medications & Supplements/Over-the-Counter

Major Pharmaceuticals Acetaminophen Tablets Recalled for Discoloration

Agency Publication Date: June 22, 2024
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Summary

Contract Pharmacal Corporation is recalling 14,616 bottles of Major Pharmaceuticals brand Extra Strength Acetaminophen 500 mg tablets (100-count) because the tablets may show brownish discoloration. The recall affects bottles from a single production lot distributed in Michigan. If you have this medication, you should check the label to see if your bottle is part of the affected batch.

Risk

The tablets exhibit an unusual brownish color rather than their standard appearance. Using discolored medication is not recommended as it may indicate a quality defect or product degradation.

What You Should Do

  1. This recall affects 100-count bottles of Major Pharmaceuticals Extra Strength Acetaminophen 500 mg Tablets with NDC 0904-6730-60 and UPC 309046730606.
  2. Identify affected bottles by looking for Lot number 368638 with an expiration date of 05/2025 printed on the label.
  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 the manufacturer, Contract Pharmacal Corporation, for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

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: Extra Strength Acetaminophen 500 MG Tablets (100-count Bottle)by Major Pharmaceuticals
Variants: 500 mg, Tablet
UPC Codes:
309046730606
Lot Numbers:
368638 (Exp. 05/2025)
NDC:
0904-6730-60

Distributed by Major Pharmaceuticals.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94675
Status: Active
Manufacturer: Contract Pharmacal Corporation
Sold By: Major Pharmaceuticals
Manufactured In: United States
Units Affected: 14,616 bottles
Distributed To: Michigan

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.