Official recall notice

FDA DrugNot Yet Classified

amazon Acetaminophen Recall (Oct 2026) – Aurobindo Pharma USA

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

Recall date
2026-10-07
Category
Drug
FDA class
Not Yet Classified

Why it was recalled

Hazard

Discoloration: consumer complaints received for discolored tablets

One email a week when there are new recalls. Confirm by email; unsubscribe anytime.

Product description

Discoloration: consumer complaints received for discolored tablets

Affected products

Lot# ACD124048A, Exp Date: 11/30/2027.

Verify with the official notice →
Share:

Related Recalls

2026-10-14 · FDA_DRUG
FDA Recall: Par Health and Endo USA: Argatroban Injection 250 mg/2.5 mL (100 mg/mL)
Par Health and Endo USA
2026-10-09 · FDA_DRUG
FDA Recall: Par Pharmaceutical: Brevital Sodium 500 mg/vial for Injection
Par Pharmaceutical
2026-10-07 · FDA_DRUG
FDA Recall: Paroxetine Extended-Release Tablets, 37.5mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc.,
Apotex Corp.
2026-10-07 · FDA_DRUG
FDA Recall: FOCUS PI Hypromellose 0.7% Formula, 0.3 FL O (10 mL) per vial, STERILE, Manufactured for: Covalent M
Aurolab Trust