RecallRadar

FDA Drug recall D-0925-2018

Admelog Solostar (insulin lispro injection), 100 units/ mL (U-100) injection, packaged in 3mL prefilled pens, 1 pen per box, Rx only, Physi…

On 2018-07-18 the FDA classified a Class II recall of Admelog Solostar (insulin lispro injection), 100 units/ mL (U-100) injection, packaged in 3mL prefilled pens, 1 pen per box, Rx only, Physi… by Sanofi Aventis U S, citing temperature Abuse: Product samples of Admelog may not have been shipped at proper temperature.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0925-2018
ClassificationClass II
Statusongoing
Initiated2018-07-05
Published2018-07-18
Last updated2026-09-13 11:52 UTC
CompanySanofi Aventis U S
DistributionUS

Product

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

Reason

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

Identifiers

ndc0024-5924-10
ndc0024-5925-01
ndc0024-5925-05
ndc0024-5925-00
ndc0024-5926-05
code_infoLot #: 7F021B, Exp 6/30/20

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0925-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.