US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 7, 2021 (5 years ago)

Sulfamethoxazole and Trimethoprim Tablets, USP, 800mg/160mg Double Strength, 500 Tablets…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Foreign Substance- Potential of metal contamination.

What was recalled

Sulfamethoxazole and Trimethoprim Tablets, USP, 800mg/160mg Double Strength, 500 Tablets, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-HIghtstown Road, EAs Windsor, NJ 08520, Made in India, NDC 65862-420-05

Recalling firm
Aurobindo Pharma USA Inc.
NDC code
65862-420-05
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0719-2021

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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