Mckesson recalls 0.15 mg epinephrine auto-injectors due to temperature abuse risks. Products may have been shipped with improper temperature control, potentially affecting safety.
cGMP deviations: Temperature abuse
Mckesson is recalling single-dose epinephrine auto-injectors that could be affected by temperature abuse. This means the products might not be safe if stored or transported outside recommended temperature ranges.
The recall is for temperature abuse, meaning the product could be affected if stored or transported outside the recommended temperature range. This might lead to improper function of the auto-injector, potentially reducing effectiveness during emergencies.
Prescription holders of the recalled epinephrine auto-injectors. People who use these injectors for emergencies are at risk if the product was exposed to improper temperatures.
Check for the product name 'Epineph: 0.15 mg single-dose auto-injectors', packaged in 2-count cartons, manufactured by Mylan Pharma with NDC 49502-101-02. The recall applies to products distributed by McKesson Medical-Surgical.
Look for the product name, packaging, and NDC number to confirm if it matches the recalled items.
The recall is due to temperature abuse risks, meaning the product could be affected if stored or transported outside recommended temperature ranges.
The official notice does not specify a remedy or action for affected products.
Check for the product name 'Epinephrine Injection, USP, Single-Dose Auto-Injectors 0.15 mg', packaged in 2-count cartons, manufactured by Mylan Pharma with NDC 49502-101-02.
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-1014-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1014-2022 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.
