LOSARTAN POTASSIUM TABLETS USP — Class II drug recall D-0253-2015
Terminated recall by Micro Labs Usa, Inc S, reported 2014-11-26, distributed in NY. Failed Content Uniformity Specifications; Dry mix failed blend uniformity.
| Recall number | D-0253-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Micro Labs Usa, Inc S, Princeton, NJ, United States |
| Recall initiated | 2014-09-22 |
| Classified | 2014-11-18 |
| Reported by FDA | 2014-11-26 |
| Terminated | 2015-12-22 |
| Distributed | NY |
| Quantity | 144 bottles |
| NDC | 42571-0110-10 |
| Lot numbers | LJAG003 |
| Expiration dates | 2015-05 |
Product
LOSARTAN POTASSIUM TABLETS USP, 25 mg, 1000 Tablet Bottles, Rx Only. Manufactured by: Micro Labs Limited, Goa-403 722, INDIA. Manufactured for: Micro Labs USA, Inc., Princeton, NJ 08540. NDC 42571-110-10
Reason for recall
Failed Content Uniformity Specifications; Dry mix failed blend uniformity.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0253-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.