PlainRecalls
FDA Drug Moderate Class II Terminated

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.

Reported: September 2, 2020 Initiated: August 10, 2020 #D-1535-2020

Product Description

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.

Reason for Recall

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

Details

Recalling Firm
Aurobindo Pharma USA Inc.
Units Affected
5748 bottles
Distribution
Nationwide in the U.S.
Location
East Windsor, NJ

Frequently Asked Questions

What product was recalled?
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.. Recalled by Aurobindo Pharma USA Inc.. Units affected: 5748 bottles.
Why was this product recalled?
Presence of Foreign Substance: product complaints were received by the firm for the presence of metal wire in the tablet(s).
Which agency issued this recall?
This recall was issued by the FDA Drug on September 2, 2020. Severity: Moderate. Recall number: D-1535-2020.