CLASS II Drug recall · Reported 2 Sep 2020 · FDA Enforcement Report

Sulfamethoxazole and Trimethoprim Tablets recalled

Aurobindo Pharma USA is recalling Sulfamethoxazole and Trimethoprim Tablets, USP, 800 mg/160 mg Double Strength per, distributed nationwide in the US. The recall was initiated on 10 Aug 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #s: STSD19109-A, Exp. 05/31/2022; SP1D19083AA3, SP1D19084AA3, Exp. 08/31/2022.
NDC65862-419, 65862-420
Quantity recalled5748 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1535-2020
FDA event ID
86190
Recalling firm
Aurobindo Pharma USA, East Windsor, NJ
Manufacturer
Aurobindo Pharma Limited
Classification
Class II
Status
Terminated
Recall initiated
10 Aug 2020
FDA classified
21 Aug 2020
Reported
2 Sep 2020
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material
Drug class
Antibiotics

Timeline

10 Aug 2020Recall initiated by company
21 Aug 2020Classified by FDA+11 days
2 Sep 2020Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Presence of Foreign Substance: product complaints were received by the firm for the presence of metal wire in the tablet(s).

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

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

Where it was distributed

Nationwide in the U.S.

Nationwide

Questions about this recall

Why was it recalled?

Presence of Foreign Substance: product complaints were received by the firm for the presence of metal wire in the tablet(s).

Which lots are affected?

Lot #s: STSD19109-A, Exp. 05/31/2022; SP1D19083AA3, SP1D19084AA3, Exp. 08/31/2022.

Where was it sold?

Nationwide in the U.S.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 14 Oct 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Aurobindo Pharma USA

All 59

Other Sulfamethoxazole recalls

All 15
ReportedClassRecallCompanyReasonWhere
DrugCLASS IISulfamethoxazole and Trimethoprim Tablets recalledSulfamethoxazole And TrimethoprimNorthwind PharmaceuticalsPackaging DefectsNationwide
DrugCLASS IISulfamethoxazole and Trimethoprim, USP, 800 mg/160 mg recalledSulfamethoxazole And TrimethoprimThe Harvard Drug GroupPackaging DefectsNationwide
DrugCLASS IISulfamethoxazole and Trimethoprim, USP, 800 mg/160 mg recalledSulfamethoxazole And TrimethoprimThe Harvard Drug GroupPackaging DefectsNationwide
DrugCLASS IISulfamethoxazole and Trimethoprim Tablets, USP 800mg/160mg recalledSulfamethoxazole And TrimethoprimAmneal PharmaceuticalsPackaging DefectsNationwide
DrugCLASS ISulfamethoxazole and Trimethoprim Tablets, USP, 400 mg/80 mg recalledSulfamethoxazole And TrimethoprimAmneal PharmaceuticalsSterilityNationwide