Mckesson Medical-Surgical recalls dihydroergotamine injections due to temperature abuse risks. This prescription drug may be unsafe if exposed to improper temperatures.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling dihydroergotamine injections that could be unsafe if exposed to improper temperatures. This recall affects prescription-only products sold through their pharmacy network.
The product was manufactured with cGMP (current Good Manufacturing Practice) deviations related to temperature abuse. This means the drug could be unstable or ineffective if stored or handled at incorrect temperatures.
Prescription patients who received this dihydroergotamine injection from a pharmacy using Mckesson Medical-Surgical. Patients with high-risk conditions like migraines may be most affected.
Check for dihydroergotamine injections labeled as 1mg/mL in a box of 5 x 1 mL ampules. This prescription drug was sold through Mckesson Medical-Surgical pharmacies. The recall covers products distributed between specific dates but the exact lot numbers are unknown.
Look for the product label showing dihydroergotamine injection, 1mg/mL, in a box of 5 x 1 mL ampules.
The recall states there were cGMP deviations related to temperature abuse, but the official notice does not specify if the product is safe to use.
Check for dihydroergotamine injections labeled as 1mg/mL in a box of 5 x 1 mL ampules. This product was distributed through Mckesson Medical-Surgical pharmacies.
The recall does not specify a remedy, so the official notice does not state what action to take.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall D-1011-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1011-2022 from Mckesson Medical-Surgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
