Amazon Extra Strength Acetaminophen Caplets
Acetaminophen Extra Strength caplets have discolored tablets, which may indicate a problem.
What happened
Aurobindo Pharma USA Inc is recalling amazon Acetaminophen Extra Strength 500mg Caplets in 200-count, 500-count, and 1000-count bottles due to consumer complaints of discolored tablets. The recall began September 18, 2026, and was added to the FDA's Enforcement Report on October 1, 2026.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Affected if its lot code and NDC or UPC are listed under that product.
amazon, Acetaminophen, Extra Strength
- Strength
- 500 mg
- NDC / UPC
- NDC 72288-692-20
- UPC 1 95515 04887 3
- Lot
- ACD125040A
- NDC / UPC
- NDC 72288-692-50
- UPC 1 95515 04890 3
- Lot
- ACD124036A
- ACD124030A
- ACD124042A
- ACD124048B
- ACD125010A
- NDC / UPC
- NDC 72288-692-01
- UPC 1 95515 04888 0
- Lot
- ACD124048A
Details
- Company began the recall
- Event ID
- 99934
- Company
- Aurobindo Pharma USA Inc
- Hazard
- Product quality defect
Company began the recall
Added to FDA's Enforcement Report
Listed on Recall Canary
Summary updated
In FDA's weekly enforcement report
