Mckesson Medical-Surgical recalls glucagon injections due to temperature abuse risks. Products may have been shipped without proper temperature control, potentially causing safety issues.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical recalls glucagon injections that could be affected by temperature abuse. This means the product might have been stored or transported improperly, leading to safety risks.
The recall is due to cGMP deviations related to temperature abuse. This means the product may have been stored or transported without maintaining the required temperature, which could affect its safety and effectiveness.
Prescription holders of glucagon injections packaged in 10-count boxes (1 mg per vial) are likely affected. Those who received the product from McKesson Medical-Surgical may be at risk if the product was exposed to improper temperatures.
Check for glucagon injections in 10-count boxes with 1 mg per vial, manufactured by Boehringer Mannheim (NDC 0597-0053-45). Products distributed by McKesson Medical-Surgical may have been affected if they were shipped without proper temperature control.
Look for glucagon injections in 10-count boxes (1 mg per vial) with NDC 0597-0053-45.
The product was recalled due to cGMP deviations related to temperature abuse, meaning it may have been stored or transported without proper temperature control.
Check for glucagon injections in 10-count boxes (1 mg per vial) with NDC 0597-0053-45, distributed by McKesson Medical-Surgical.
The recall does not specify a remedy, so you should contact your healthcare provider for guidance.
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-1038-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1038-2022 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.
