HydrALAZINE Hydrochloride Tablets — Class II drug recall D-0332-2015
Terminated recall by Par Pharmaceutical Inc., reported 2015-01-14, distributed nationwide. Presence of Foreign Substance: Par Pharmaceutical, Inc. is recalling one lot of HydrALAZINE Hydrochloride tabl
| Recall number | D-0332-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Par Pharmaceutical Inc., Spring Valley, NY, United States |
| Recall initiated | 2014-11-24 |
| Classified | 2015-01-06 |
| Reported by FDA | 2015-01-14 |
| Terminated | 2017-05-01 |
| Distributed | Nationwide (US) |
| Quantity | 38,788 bottles |
| Lot numbers | 01/17, 26708501 |
Product
HydrALAZINE Hydrochloride Tablets, USP 25 mg, 100 count bottle Rx only, Distributed by: Par Pharmaceutical Companies, Inc. Spring Valley, NY10977
Reason for recall
Presence of Foreign Substance: Par Pharmaceutical, Inc. is recalling one lot of HydrALAZINE Hydrochloride tablets due to the presence of small aluminum particles.
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-0332-2015. 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.