Sanofi recalls Admelog insulin vials with malformed crimped collar seals that could lead to contamination. Affected vials have NDC 0024-5926-05 and lot # 3F497B, expiring Dec 2025.
Lack of Assurance of Sterility: Malformed crimped collar seal
Sanofi is recalling Admelog insulin vials that may have a malformed crimped collar seal, which could allow contamination. This recall affects people using insulin injections and requires immediate action to prevent potential infection.
The vial's crimped collar seal may be malformed, creating a gap that could allow contaminants to enter the insulin. This could lead to infection if the vial is used after the seal fails.
People with diabetes who use Admelog insulin vials are affected. Those using the recalled vials are at risk of contamination if the seal fails.
Check for NDC code 0024-5926-05 and lot number 3F497B on the vial label. The vials expire December 2025.
Look for NDC 0024-5926-05 and lot # 3F497B on the vial label.
No, this recall is specific to Admelog insulin vials with NDC 0024-5926-05 and lot # 3F497B.
The recall record does not specify a remedy, so contact Sanofi for guidance.
The vials expire December 31, 2025.
We’ve drafted a message you can send Sanofi to request your refund or repair — edit it as you like.
Subject: Recall D-0575-2023 — Sanofi Sanofi Hello, I own a Sanofi that is covered by recall D-0575-2023 from Sanofi. 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.
