Risedronate recalls
The FDA has published 3 recalls involving Risedronate since 2017. The latest was reported on 13 Apr 2022. Most were for potency & assay. Teva Pharmaceuticals U has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls3since 2017
Last 12 months0reported
Class I00% of total
Ongoing0latest 13 Apr 2022
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 0 0%Class III 3 100%
Why risedronate is recalled
Companies
By year
All risedronate recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Risedronate Sodium Tablets, USP, 5 mg recalled by Macleods Pharma UsaRisedronate Sodium | Macleods Pharma Usa | Other | Nationwide |
| Drug | CLASS III | Risedronate Sodium Delayed-release Tablets, 35 mg recalled | Teva Pharmaceuticals U | Potency & Assay | Nationwide |
| Drug | CLASS III | Risedronate Sodium Delayed-release Tablets, 35 mg recalled | Teva Pharmaceuticals U | Potency & Assay | Nationwide |
Should you stop taking Risedronate?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.