Loperamide Hydrochloride recalls
Loperamide Hydrochloride products have been recalled 2 times, most recently on 15 Jun 2022. The recalling company is usually Sun Pharmaceutical Industries. The most common reason is manufacturing (cgmp) deviations.
Total recalls2since 2019
Last 12 months0reported
Class I00% of total
Ongoing0latest 15 Jun 2022
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 50%Class III 1 50%
Why loperamide hydrochloride is recalled
Companies
Product types
By year
All loperamide hydrochloride recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Loperamide Hydrochloride capsules, USP, 2 mg recalledLoperamide Hydrochloride | Mckesson Medical-Surgical Inc. Corporate Office | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Loperamide HCL Tablets USP, 2 mg, Anti-diarrheal, 24 caplets recalledLoperamide Hydrochloride | Sun Pharmaceutical Industries | Other | OH |
About 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.