Mckesson recalls Adrenalin epinephrine injection vials due to temperature abuse risks. This affects prescription products from Par Pharma with specific NDC numbers. Consumers should check their prescription details for affected lots.
cGMP deviations: Temperature abuse
Mck:ckesson Medical-Surgical recalls Adrenalin epinephrine injection vials (30 mg/30 mL) due to potential temperature abuse. This could lead to unsafe drug concentrations if the product is exposed to improper temperatures during storage or transport.
Temperature abuse means the product may have been exposed to temperatures outside the safe range during storage or transport. This could cause the epinephrine concentration to become unsafe for medical use, potentially leading to ineffective treatment during emergencies.
Prescription holders of Adrenalin epinephrine injection vials from Par Pharma with NDC 42023-168-01. Those who have received the product through McKesson Medical-Surgical are most at risk.
Check your prescription details for the NDC number 42023-168-01. The product is a 30 mL multiple-dose vial of epinephrine injection, prescription-only, manufactured by Par Pharma.
Review your prescription for the NDC number 42023-168-01 to confirm if you have the recalled product.
The product was recalled due to cGMP deviations related to temperature abuse, which could affect the safety of the epinephrine concentration.
Check your prescription for the NDC number 42023-168-01. The product is a 30 mL multiple-dose vial of epinephrine injection, prescription-only, manufactured by Par Pharma.
The recall record does not specify a remedy, so contact your healthcare provider or pharmacist 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-1022-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1022-2022 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.
