Sanofi-Aventis U.S. LLC recalls Admelog Solostar (insulin lispro injection), 100 units/ mL (U-100) injection, packaged in 3mL prefilled pens, 1 pen per
Sanofi recalls Admelog Solostar insulin pens that may not have been shipped at proper temperature, risking insulin effectiveness. Affected units include specific lot numbers and expiration dates.
Lower-risk recall
Temperature Abuse: Product samples of Admelog may not have been shipped at proper temperature.
Contact the company & request your remedy
What happened, in plain English
Sanofi is recalling Admelog Solostar insulin pens that may have been improperly shipped, potentially affecting insulin effectiveness. This recall is for specific lot numbers and expiration dates. Read more at govinfonow.com/recall/40382-sanofi-admelog-solostar-insulin-pens-recalled-due-to-temperature-abuse.
Source Summary by GovInfoNow · govinfonow.com/recall/40382-sanofi-admelog-solostar-insulin-pens-recalled-due-to-temperature-abuse · Updated October 6, 2026 · FDA enforcement record: FDA #D-0925-2018
Cite this page
“Sanofi Admelog Solostar insulin pens recalled due to temperature abuse risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/40382-sanofi-admelog-solostar-insulin-pens-recalled-due-to-temperature-abuse. Based on FDA recall #D-0925-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0925-2018%22&limit=1).
Why it’s dangerous
Insulin pens require proper temperature control during shipping and storage to maintain effectiveness. If the product was not shipped at the correct temperature, the insulin may become less effective, potentially leading to inconsistent blood sugar management.
Who’s affected
People with diabetes who use Admelog Solostar insulin pens, particularly those with the specific lot number 7F021B and expiration date 6/30/2020.
How to tell if you have this one
Check for the lot number 7F021B and expiration date 6/30/2020 on the pen packaging. The product is a 3mL prefilled insulin pen sold by prescription only.
- Brand
Sanofi- Category
Drug
What to do — step by step
Check Pen Details
Look for the lot number 7F021B and expiration date 6/30/2020 on the pen packaging.
Questions people ask
Is this product safe to use?
The recall is for specific units that may not have been shipped at proper temperature. If your pen has the lot number 7F021B and expires 6/30/2020, it may not be effective and should be checked.
What should I do if I have this product?
Check the lot number and expiration date on the pen packaging. If it matches 7F021B and expires 6/30/2020, contact Sanofi for guidance.
How can I get a replacement?
The recall record does not specify a replacement process. Contact Sanofi directly for assistance.
Contact Sanofi
We’ve drafted a message you can send Sanofi to request your refund or repair — edit it as you like.
Subject: Recall D-0925-2018 — Sanofi Sanofi Hello, I own a Sanofi that is covered by recall D-0925-2018 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.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
Where this comes from
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.
- Official source: FDA Recall #D-0925-2018 (July 5, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0925-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.