Mckesson recalls Glucagon Emergency Kits due to temperature abuse risks. This affects prescription products with NDC 0002-8031-01. Consumers should check if their kit was distributed between specific dates.
cGMP deviations: Temperature abuse
Mckesson is recalling prescription Glucagon Emergency Kits because of temperature abuse risks. This could lead to ineffective treatment for low blood sugar emergencies if the kit is exposed to improper temperatures.
The Glucagon Emergency Kit can become ineffective if exposed to temperatures outside the recommended range. This could happen if the kit is stored or transported in conditions that cause temperature abuse, such as leaving it in a hot car or near a heat source.
People with prescriptions for Glucagon Emergency Kits are affected. Those who received the kit from McKesson Medical-Surgical between the dates mentioned in the recall are most at risk.
Check for the NDC code 0002-8031-01 on the kit. The recall includes prescription products distributed by McKesson Medical-Surgical between specific dates mentioned in the recall notice.
Look for the NDC code 0002-8031-01 on the Glucagon Emergency Kit packaging.
Ask your pharmacist if you have the recalled Glucagon Emergency Kit with NDC 0002-8031-01.
The recall is due to temperature abuse risks, which could make the kit ineffective for treating low blood sugar emergencies.
Check for the NDC code 0002-8031-01 on the kit. The recall includes products distributed by McKesson Medical-Surgical between specific dates mentioned in the notice.
Contact your pharmacist to confirm if you have the recalled kit. They can advise on next steps.
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-1051-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1051-2022 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.
