Drug recall D-1535-2020
Product
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).
Lots and codes
Lot #s: STSD19109-A, Exp. 05/31/2022; SP1D19083AA3, SP1D19084AA3, Exp. 08/31/2022.
Recall details
- Recalling firm
- Aurobindo Pharma USA Inc., East Windsor, NJ
- Quantity
- 5748 bottles
- Distribution
- Nationwide in the U.S.
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 10, 2020
- Terminated
- June 28, 2024
Related products
- Sulfamethoxazole and Trimethoprim – drug information
- NDC 65862-420 Sulfamethoxazole and Trimethoprim · Sulfamethoxazole 800 mg/1; Trimethoprim 160 mg/1 · Aurobindo Pharma Limited
- NDC 65862-419 Sulfamethoxazole and Trimethoprim · Sulfamethoxazole 400 mg/1; Trimethoprim 80 mg/1 · Aurobindo Pharma Limited