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
Reported: May 25, 2022 Initiated: April 5, 2022 #D-0882-2022
Product Description
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
Reason for Recall
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.
Details
- Recalling Firm
- Cardinal Health Inc.
- Units Affected
- 1 box
- Distribution
- NM only
- Location
- Dublin, OH
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Cardinal Health Inc.. Units affected: 1 box.
Why was this product recalled? ▼
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 25, 2022. Severity: Critical. Recall number: D-0882-2022.
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