Pro recalls
The FDA has published 2 recalls involving Pro since 2016. The latest was reported on 22 Aug 2018. Most were for labeling errors. Ranier's Compounding Laboratory 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 recalls2since 2016
Last 12 months0reported
Class I150% of total
Ongoing0latest 22 Aug 2018
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 1 50%Class II 1 50%Class III 0 0%
Why pro is recalled
Companies
By year
All pro recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | PRO/PA/PH/AT 18mcg/1.8mg/ (Prostaglandin//Papaverine/Phentol recalled | Ranier's Compounding Laboratory | Sterility | PA |
| Drug | CLASS I | PRO capsules, Proprietary Blend, 350 mg recalled by Ultimate Body Tox | Ultimate Body Tox | Labeling Errors | Nationwide |
Should you stop taking Pro?
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.