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FDAFDA · Food and drugs·Recall number D-0882-2022

Humalog KwikPen, Insulin lispro injection, U-100, 100 units per mL, 5x3 mL Prefilled Pens per box, Marketed by Lilly USA, LLC, Indianapolis, IN 46285, Box NDC 0002-8799-59, Pen NDC 002-7516-59

Published May 25, 2022 · Recall initiated: April 5, 2022

Status when published: Completed — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
HUMALOG
Manufacturer
Cardinal Health Inc.
Distributor
NM only
Lot
Unknown
Risk classification
Class I
Area (FDA)
drug
Country
United States

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