Dabigatran etexilate Capsules — Class III drug recall D-0736-2026
Ongoing recall by Ascend Laboratories, LLC, reported 2026-07-29, distributed nationwide. Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analys
| Recall number | D-0736-2026 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ascend Laboratories, LLC, Bedminster, NJ, United States |
| Recall initiated | 2026-06-30 |
| Classified | 2026-08-04 |
| Reported by FDA | 2026-07-29 |
| Distributed | Nationwide (US) |
| Quantity | 2,717 cartons |
| Reason classes | specification failure |
| NDC | 00904-7253, 00904-7253-04, 00904-7253-35, 00904-7253-68, 00904-7254, 00904-7254-35, 00904-7254-68, 00904-7255, 00904-7255-10, 00904-7255-35, 00904-7255-68 |
| Lot numbers | 25141584 |
| Expiration dates | 2027-04-30 |
Product
Dabigatran etexilate Capsules, 150 mg, 20-count carton (2x10), Rx only, Manufactured by: Alkem Laboratories, Mumbai, INDIA, Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC 0904-7255-10.
Reason for recall
Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and Total impurity testing for 12 Month Long-Term Stability.
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-0736-2026. 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.