Not Yet ClassifiedDrug
amazon recall
Summary
Aurobindo Pharma USA Inc is recalling amazon (drug). According to the FDA report, the reason is: Discoloration: consumer complaints received for discolored tablets. The FDA rated this a Not Yet Classified: Recall status: Ongoing.
Details from the FDA report
- Product
- amazon, Acetaminophen, Extra Strength, 500mg Caplets, 1000-count bottle, Distributed by: Amazon.com Services LLC, 410 Terry Avenue N., Seattle, WA 98109, Made in India, NDC 72288-692-01. UPC 1 95515 04888 0
- Reason
- Discoloration: consumer complaints received for discolored tablets
- Lot / code info
- Lot# ACD124048A, Exp Date: 11/30/2027.
- Quantity
- 7,836 1000-count bottles
- Distribution
- US Nationwide.
- Recalling company
- Aurobindo Pharma USA Inc, East Windsor, NJ United States
- Recall started
- September 18, 2026
- FDA report date
- October 7, 2026
- Classification
- Not Yet Classified:
- Voluntary / mandated
- Voluntary: Firm initiated
- Status
- Ongoing
- Recall number
What to do
- Check whether you have this product, and compare the lot numbers, codes, or dates on your package with the codes listed above.
- If it matches, stop using it and keep it away from children and pets.
- Contact the recalling company (Aurobindo Pharma USA Inc) or the store where you bought it about returns or refunds.
- Do not stop a prescribed medication without first talking to your pharmacist or doctor; they can help find a safe replacement.
- If you think the product made you or someone else sick, contact a doctor or pharmacist. In an emergency call 911.
- You can report problems to the FDA via MedWatch.