Ranitidine Hydrochloride recalls
Ranitidine Hydrochloride products have been recalled 2 times, most recently on 13 Nov 2019. The recalling company is usually Dr. Reddy's Laboratories. The most common reason is nitrosamine impurity.
Total recalls2since 2019
Last 12 months0reported
Class I00% of total
Ongoing0latest 13 Nov 2019
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 100%Class III 0 0%
Why ranitidine hydrochloride is recalled
Companies
Product types
By year
All ranitidine hydrochloride recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Dr. Reddy's Ranitidine Capsules, USP 300 mg, a.) bottles recalledRanitidine Hydrochloride | Dr. Reddy's Laboratories | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Dr. Reddy's: Ranitidine Capsules 150 mg, Rx a.) bottles recalledRanitidine Hydrochloride | Dr. Reddy's Laboratories | Nitrosamine Impurity | Nationwide |
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.