Mckesson Medical-Surgical recalls Sumatriptan 6mg injections due to temperature abuse risks. Patients should check if their prescription vials were shipped with improper temperature control.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Sumatriptan 6mg injections because they may have been exposed to improper temperatures during shipping. This could lead to ineffective or unsafe medication use for patients needing acute migraine treatment.
The product may have been exposed to temperatures outside the recommended range during shipping, which could affect the medication's stability and effectiveness. This might result in the injection not working properly or causing unintended side effects when used.
Patients with a prescription for Sumatriptan 6mg injections who received the product from a pharmacy that distributed it after the recall date. Those using the medication for migraine relief are most at risk if the product was improperly stored.
Check your prescription vials for the manufacturer's label: Auromedics Pharma LLC, NDC 55150-0173-01. The product was shipped in boxes of 5 single-dose vials, each containing 0.5 mL of 6mg Sumatriptan.
Look for the manufacturer label: Auromedics Pharma LLC, NDC 55150-0173-01 on the vial packaging.
The recall indicates potential temperature abuse during shipping, which might affect the medication's effectiveness. It is not safe to use without confirming the product was shipped with proper temperature control.
Check for the manufacturer label: Auromedics Pharma LLC, NDC 55150-0173-01 on the vial packaging. The product comes in boxes of 5 single-dose vials.
The recall does not require immediate discontinuation; however, you should check the product label to confirm if it was shipped with proper temperature control before use.
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-1007-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1007-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
