Contract Pharmacal Corporation recalls 100-count Extra Strength Acetaminophen 500mg tablets with brownish discoloration. This may indicate a manufacturing issue. Consumers should check product details and contact the manufacturer for guidance.
Discoloration: Brownish tablets
Contract Pharmacal Corporation is recalling 100-count bottles of Extra Strength Acetaminophen 500mg tablets due to brownish discoloration. This discoloration could indicate a manufacturing issue that may affect product safety. Consumers should check their product details and contact the manufacturer if unsure.
Brownish discoloration in the tablets may indicate a manufacturing issue that could affect product safety. While the hazard is not described as causing serious injury, the discoloration suggests a potential problem with the tablet's composition.
People who own or use the 100-count Extra Strength Acetaminophen 500mg tablets distributed by Major Pharmaceuticals. Those most at risk are individuals who have the specific lot number or expiration date.
Check for brownish discoloration on the tablets. The affected product has a lot number of 368638 and expires May 2025. It was distributed by Major Pharmaceuticals.
Look for brownish discoloration on the tablets and verify the lot number (368638) and expiration date (May 2025).
The recall is due to brownish discoloration, which may indicate a manufacturing issue. The official notice does not specify if the product is unsafe to use.
Check for brownish discoloration on the tablets and verify the lot number (368638) and expiration date (May 2025).
The recall does not specify a remedy, so contact the manufacturer for guidance if you have the product with brownish discoloration.
We’ve drafted a message you can send Contract Pharmacal Corporation to request your refund or repair — edit it as you like.
Subject: Recall D-0566-2024 — Contract Pharmacal Corporation Contract Pharmacal Corporation Hello, I own a Contract Pharmacal Corporation that is covered by recall D-0566-2024 from Contract Pharmacal Corporation. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
