Melanotan Ii recalls
The FDA has published 2 recalls involving Melanotan Ii since 2019. The latest was reported on 27 Apr 2022. Most were for sterility. North American Custom Laboratories 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 2019
Last 12 months0reported
Class I00% of total
Ongoing0latest 27 Apr 2022
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 100%Class III 0 0%
Why melanotan ii is recalled
Companies
By year
All melanotan ii recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Melanotan II 1 mg/mL Injection vials recalled by North American Custom | North American Custom Laboratories | Sterility | Nationwide |
| Drug | CLASS II | Melanotan II, 10mg injection recalled by Promise Pharmacy | Promise Pharmacy | Sterility | Nationwide |
Should you stop taking Melanotan Ii?
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.