Trimix Alprostadil recalls
The FDA has published 3 recalls involving Trimix Alprostadil since 2018. The latest was reported on 23 Mar 2022. Most were for sterility. Family Pharmacy of Statesville 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 2018
Last 12 months0reported
Class I00% of total
Ongoing0latest 23 Mar 2022
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 trimix alprostadil is recalled
Companies
By year
All trimix alprostadil recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Trimix (Alprostadil/Papaverine/Phentolamine) 20 mcg/30 recalled | Family Pharmacy of Statesville | Sterility | NC |
| Drug | CLASS II | Trimix (Alprostadil/Papaverine/Phentolamine) 10 mcg/20 mg/1 recalled | Family Pharmacy of Statesville | Sterility | NC |
| Drug | CLASS II | Trimix Alprostadil/ Phentolamine/Papavarin 40 mcg/1 mg/30 recalled | Pharm D Solutions | Sterility | Nationwide |
Should you stop taking Trimix Alprostadil?
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.