Pramipexole Dihydrochloridetablets recalls
The FDA has published 1 recall involving Pramipexole Dihydrochloridetablets since 2019. The latest was reported on 26 Jun 2019. Most were for manufacturing (cgmp) deviations. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls1since 2019
Last 12 months0reported
Class I00% of total
Ongoing0latest 26 Jun 2019
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 100%Class III 0 0%
Why pramipexole dihydrochloridetablets is recalled
Companies
By year
All pramipexole dihydrochloridetablets recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Pramipexole DihydrochlorideTablets 0.125 mg recalled | Zydus Pharmaceuticals USA | Manufacturing (CGMP) Deviations | Nationwide |
Should you stop taking Pramipexole Dihydrochloridetablets?
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.