US Drug Recall Register
Class I · High risk Terminated Initiated Jul 5, 2022 (4 years ago)

Insulin Glargine (Insulin glargine-yfgn) Injection, 100 units/mL (U-100), 3 mL prefilled…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Labeling: Missing label: Label missing from some prefilled pens.

What was recalled

Insulin Glargine (Insulin glargine-yfgn) Injection, 100 units/mL (U-100), 3 mL prefilled pens (NDC 49502-394-71), packaged in cartons of 5 prefilled pens (NDC 49502-394-75), Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 15317, Manufactured for: Mylan Specialty L.P., Morgantown, WV

Recalling firm
Mylan Pharmaceuticals Inc
NDC code
49502-394-71
Origin
WV, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1292-2022

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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