Dihydroergotamine recalls
The FDA has published 4 recalls involving Dihydroergotamine since 2014. The latest was reported on 25 Dec 2024. Most were for sterility. Provepharm 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 recalls4since 2014
Last 12 months0reported
Class I00% of total
Ongoing1latest 25 Dec 2024
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 4 100%Class III 0 0%
Why dihydroergotamine is recalled
Companies
By year
Ongoing dihydroergotamine recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Dihydroergotamine Mesylate Injection, solution recalled by ProvepharmDihydroergotamine Mesylate | Provepharm | Other | Nationwide |
All dihydroergotamine recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Dihydroergotamine Mesylate Injection, solution recalled by ProvepharmDihydroergotamine Mesylate | Provepharm | Other | Nationwide |
| Drug | CLASS II | Dihydroergotamine Mesylate, Injection, USP, 1mg/mL recalled | Mckesson Medical-Surgical Inc. Corporate Office | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Dihydroergotamine Mesylate, Injectable Solution, 1 MG/ML syringe recalled | JD & SN Inc | Sterility | Nationwide |
| Drug | CLASS II | Dihydroergotamine mesylate 1 mg/mL injection solution recalled | Martin Avenue Pharmacy | Sterility | Nationwide |
Should you stop taking Dihydroergotamine?
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.