Mckesson Medical-Surgical recalls EPI-PEN 2-PAK epinephrine injectors due to temperature abuse during storage. Affected units were distributed between June 1 and September 30, 2021. Consignees must check records to identify impacted products.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling EPI-PEN 2-PAK epinephrine injectors that may have been exposed to improper temperatures. This could affect the product's effectiveness in emergencies. Affected consignees should check their records to see if they received these products between June 1 and September 30, 2021.
The recall is for products that may have been exposed to improper temperatures during storage. This could affect the product's effectiveness in emergencies. The hazard is related to temperature abuse, not immediate harm to users.
Healthcare facilities and pharmacies that received EPI-PEN 2-PAK products from Mckesson Medical-Surgical between June 1 and September 30, 2021. Individuals with epinephrine auto-injectors for emergency use are most at risk if they have the recalled products.
Check if your pharmacy or healthcare facility received EPI-PEN 2-PAK products from Mckesson Medical-Surgical between June 1 and September 30, 2021. The product is labeled as 'EPI-PEN 2-PAK (epinephrine injection, USP), Single-Dose Auto-Injectors 0.3 mg, Rx only'.
Consignees should use their own records to determine if they received impacted products from Mckesson Medical-Surgical between June 1 and September 30, 2021.
The recall does not require stopping use; consignees should check records to identify impacted products.
Check if your pharmacy or healthcare facility received EPI-PEN 2-PAK products from Mckesson Medical-Surgical between June 1 and September 30, 2021.
Consignees should contact Sedgwick for assistance if they have questions about the recall.
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-0993-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-0993-2022 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.
