Rasagiline recalls
The FDA has published 3 recalls involving Rasagiline since 2014. The latest was reported on 27 Sep 2023. Most were for labeling errors. Aurobindo Pharma USA 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 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 27 Sep 2023
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why rasagiline is recalled
Companies
By year
All rasagiline recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Rasagiline Tablets 0.5mg recalled by Aurobindo Pharma USA | Aurobindo Pharma USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Rasagiline Mesylate Tablets 1 mg; in HDPE recalledRasagiline | Ascend Laboratories | Other | 20 states |
| Drug | CLASS II | Rasagiline Mesylate, Tablet, 0.5 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
Should you stop taking Rasagiline?
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.