# FDA recall D-0882-2022

> **Cardinal Health Inc.** · Class I · drug recall initiated 2022-04-05.

## Product

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.

## Distribution

NM only

## Key facts

- **Recall number:** D-0882-2022
- **Recalling firm:** Cardinal Health Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Completed
- **Initiation date:** 2022-04-05
- **Report date:** 2022-05-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dublin, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0882-2022

## Citation

> AI Analytics. FDA recall D-0882-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0882-2022. Source: US FDA. Licensed CC0.

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