HYDROCHLOROTHIAZIDE CAPSULES — Class II drug recall D-0232-2016
Terminated recall by Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals, reported 2015-11-25, distributed nationwide. Presence of Particulate Matter.
| Recall number | D-0232-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals, Huntsville, AL, United States |
| Recall initiated | 2015-10-07 |
| Classified | 2015-11-13 |
| Reported by FDA | 2015-11-25 |
| Terminated | 2016-11-16 |
| Distributed | Nationwide (US) |
| Quantity | 912 hdpe |
| Reason classes | specification failure |
| NDC | 00603-3855-93 |
Product
HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35811, NDC: 0603-3855-93.
Reason for recall
Presence of Particulate Matter.
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-0232-2016. 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.