Class II · Moderate risk
Dihydroergotamine Mesylate Injection
Discoloration
Is Dihydroergotamine recalled?
Yes — there is an active recall. 1 ongoing FDA recall mention Dihydroergotamine (4 total). Check the affected lots below.
Most common reason: Sterility / contamination (2 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Dihydroergotamine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Dihydroergotamine recalls on record
none so far in 2026; 4 on record, newest first
Class II · Moderate risk
Dihydroergotamine Mesylate
cGMP deviations: Temperature abuse
Class II · Moderate risk
Dihydroergotamine Mesylate
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Class II · Moderate risk
Dihydroergotamine mesylate 1 mg/mL injection solution packaged in…
Lack of Assurance of Sterility: Martin Avenue Pharmacy, Inc. is conducting a voluntary recall of all compounded sterile preparations within expiry. The recall is being initiated in connection with a recent FDA inspection due to observations associated with certain quality control procedures that present a risk to sterility assurance.
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