Tri-mix St2 recalls
The FDA has published 3 recalls involving Tri-mix St2 since 2014. The latest was reported on 23 Sep 2015. Most were for sterility. The Compounding Pharmacy of America 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 23 Sep 2015
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 tri-mix st2 is recalled
Companies
By year
All tri-mix st2 recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Tri-Mix ST2 (30 mg/3 mg/100 mcg) Injectable recalled | The Compounding Pharmacy of America | Sterility | Nationwide |
| Drug | CLASS II | Tri-Mix ST2/LIDO2/PGE2 0.2/0.1/0.04, Injectable recalled | The Compounding Pharmacy of America | Sterility | Nationwide |
| Drug | CLASS II | Tri-mix ST2, 30 mg/3 mg/100 mcg/mL (papaverine recalled | Martin Avenue Pharmacy | Sterility | Nationwide |
Should you stop taking Tri-mix St2?
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.