Pfizer recalls epinephrine injection vials with lot numbers LY3681, LY4360, LY4416 due to lack of sterility assurance. These vials may cause infection if used.
Lack of Assurance of Sterility.
Pfizer is recalling epinephrine injection vials that could be contaminated, posing a risk of infection if used. This recall affects specific lot numbers distributed by Hospira.
The vials lack assurance of sterility, meaning they could contain harmful bacteria or other contaminants. If injected, this could lead to infection or other health issues.
People with prescriptions for epinephrine injections who received vials with lot numbers LY3681, LY4360, or LY4416 are affected. Those using the product for medical emergencies are at higher risk.
Check the vial label for the product name 'Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL)' and lot numbers LY3681, LY4360, or LY4416. These vials were distributed by Hospira in the US.
Look for lot numbers LY3681, LY4360, or LY4416 on the vial label.
The vials lack assurance of sterility, which could lead to contamination and infection if used.
Check the vial label for the product name 'Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL)' and lot numbers LY3681, LY4360, or LY4416.
The recall does not specify a stop-use instruction; check the label for lot numbers to determine if they are affected.
We’ve drafted a message you can send Pfizer to request your refund or repair — edit it as you like.
Subject: Recall D-0590-2025 — Pfizer Pfizer Hello, I own a Pfizer that is covered by recall D-0590-2025 from Pfizer. 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.
