Diltiazem HCl Extended-Release Capsules — Class III drug recall D-1187-2018
Terminated recall by Mylan Pharmaceuticals Inc., reported 2018-09-19, distributed nationwide. Failed Impurities/Degradation Specifications: Out of specification test results obtained during routine stabil
| Recall number | D-1187-2018 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mylan Pharmaceuticals Inc., Morgantown, WV, United States |
| Recall initiated | 2018-08-07 |
| Classified | 2018-09-10 |
| Reported by FDA | 2018-09-19 |
| Terminated | 2019-08-14 |
| Distributed | Nationwide (US) |
| Reason classes | specification failure |
| NDC | 00378-5220-05 |
| Lot numbers | 3093163 |
| Expiration dates | 2019-04 |
Product
Diltiazem HCl Extended-Release Capsules, USP 120 mg 500-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505. NDC 0378-5220-05
Reason for recall
Failed Impurities/Degradation Specifications: Out of specification test results obtained during routine stability testing for related compound.
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-1187-2018. 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.