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FDA recall 99934: Aurobindo Pharma USA Inc: amazon

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FDARecall 99934Medicines

What to do

The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.

Read the official notice on accessdata.fda.gov (opens in a new tab)

Hazard

Why it was recalled

Discoloration: consumer complaints received for discolored tablets
Text from FDA, unedited.

FDA classification: Not Yet Classified. Status: Ongoing.

Is it yours? Products and codes

  • 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

    Lot or code
    Lot# ACD124048A, Exp Date: 11/30/2027.
    Quantity
    7,836 1000-count bottles

Distribution (FDA): US Nationwide.

About this record

Issued by
U.S. Food and Drug Administration
Firm
Aurobindo Pharma USA Inc
Title
Composed by Recalls Watch from fields of the record; FDA records have no title.

If someone was hurt or swallowed something: call 911, or Poison Help at 1-800-222-1222.

About this recall

What is the hazard?

FDA states: “Discoloration: consumer complaints received for discolored tablets”

What should I do if I have this product?

The FDA record of this recall has no instruction for consumers. Compare the lot codes on the notice with your product and follow the notice of the firm. The official report is linked on this page.

How do I know if my product is included?

Compare the lot or code printed on your product with the codes FDA lists on this notice, product by product.

When was this recall published?

FDA published recall 99934 on October 7, 2026.

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