Quad Mix 1 recalls
The FDA has published 3 recalls involving Quad Mix 1 since 2014. The latest was reported on 24 May 2017. 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 24 May 2017
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 quad mix 1 is recalled
Companies
By year
All quad mix 1 recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | QUAD MIX 1/30/0.5/0.1 MDV MCG/MG/MG/MG/ML INJ, Injection recalled | Key Pharmacy and Compounding Center | Sterility | Nationwide |
| Drug | CLASS II | Quad-Mix 1 Injectable, Multi-Dose Vial, Sterile recalled | The Compounding Pharmacy of America | Sterility | Nationwide |
| Drug | CLASS II | Quad mix 1, 12 mg/1 mg/10 mcg/0.15 mg/mL (papaverine recalled | Martin Avenue Pharmacy | Sterility | Nationwide |
Should you stop taking Quad Mix 1?
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.