Aurobindo Pharma recalls 325mg acetaminophen tablets with brown surface discoloration due to manufacturing issues. Consumers should check NDC 72288-405-10 and lot number AEF124004A for affected products.
cGMP deviations: Due to confirmed consumer complaints received with the observation of tablet discoloration (brown surface on tablets).
Aurobindo Pharma is recalling 325mg acetaminophen tablets that have been reported to develop brown discoloration on the surface. This discoloration is linked to manufacturing deviations that could affect product safety.
The tablets show brown discoloration on their surface due to confirmed manufacturing deviations. This discoloration is reported by consumers and indicates potential quality issues that could affect product safety.
People who purchased the 325mg acetaminophen tablets with NDC 72288-405-10 and lot number AEF124004A from Amazon.com are affected. Those with the brown discoloration on tablets are most at risk.
Check for brown discoloration on the surface of the tablets. Affected products have NDC 72288-405-10 and lot number AEF124004A, distributed through Amazon.com.
Inspect the tablets for brown discoloration on the surface.
The recall is due to confirmed consumer complaints about tablet discoloration (brown surface) linked to manufacturing deviations.
The official notice does not specify a remedy for this recall, so contact Aurobindo Pharma for further instructions.
Check for brown discoloration on the surface of the tablets. Affected products have NDC 72288-405-10 and lot number AEF124004A, distributed through Amazon.com.
We’ve drafted a message you can send Aurobindo Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0471-2025 — Aurobindo Pharma Aurobindo Pharma Hello, I own a Aurobindo Pharma that is covered by recall D-0471-2025 from Aurobindo Pharma. 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.
