Pramipexole Di-hcl recalls
The FDA has published 4 recalls involving Pramipexole Di-hcl since 2014. The latest was reported on 22 Jan 2014. Most were for labeling errors. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls4since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 22 Jan 2014
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 4 100%Class III 0 0%
Why pramipexole di-hcl is recalled
Companies
By year
All pramipexole di-hcl recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Pramipexole Di-hcl, Tablet, 0.125 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
| Drug | CLASS II | Pramipexole Di-hcl Tablet, 0.25 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
| Drug | CLASS II | Pramipexole Di-hcl Tablet, 1 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
| Drug | CLASS II | Pramipexole Di-hcl, Tablet, 1.5 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
Should you stop taking Pramipexole Di-hcl?
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.