Diltiazem Hydrochloride recalls
Diltiazem Hydrochloride products have been recalled 7 times, most recently on 16 Apr 2025. The recalling company is usually Glenmark Pharmaceuticals Inc., U. The most common reason is nitrosamine impurity.
Total recalls7since 2023
Last 12 months0reported
Class I00% of total
Ongoing6latest 16 Apr 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 7 100%Class III 0 0%
Why diltiazem hydrochloride is recalled
Companies
Product types
By year
Ongoing diltiazem hydrochloride recalls
6 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Diltiazem Hydrochloride Extended-Release Capsules 12HR recalledDiltiazem Hydrochloride | Glenmark Pharmaceuticals Inc., U | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Diltiazem Hydrochloride Extended-Release Capsules, USP 90 mg recalledDiltiazem Hydrochloride | Glenmark Pharmaceuticals Inc., U | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Diltiazem Hydrochloride Extended-Release Capsules recalledDiltiazem Hydrochloride | Glenmark Pharmaceuticals Inc., U | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg recalledDiltiazem Hydrochloride | Glenmark Pharmaceuticals Inc., U | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Diltiazem Hydrochloride Extended-Release Capsules recalledDiltiazem Hydrochloride | Glenmark Pharmaceuticals Inc., U | Potency & Assay | Nationwide |
| Drug | CLASS II | Diltiazem Hydrochloride Extended-Release Capsules recalledDiltiazem Hydrochloride | Glenmark Pharmaceuticals Inc., U | Potency & Assay | Nationwide |
All diltiazem hydrochloride recalls, newest first
7 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.