US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jul 5, 2018 (8 years ago)

Admelog Solostar (insulin lispro injection), 100 units/ mL (U-100) injection, packaged in…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Temperature Abuse: Product samples of Admelog may not have been shipped at proper temperature.

What was recalled

Admelog Solostar (insulin lispro injection), 100 units/ mL (U-100) injection, packaged in 3mL prefilled pens, 1 pen per box, Rx only, Physician Sample - Not For Sale, Sanofi-Aventis U.S. LLC, Bridgewater, NJ 08807, NDC 0024-5925-00

Recalling firm
Sanofi-Aventis U.S. LLC
NDC code
0024-5925-00
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0925-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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