# FDA recall Z-0466-2025

> **Smiths Medical ASD, Inc.** · Class II · device recall initiated 2024-06-26.

## Product

smiths medical CADD-Solis Li-ion Rechargeable Battery Packs AC adapter, Model Number REF 21-0270-25, for use with the CADD-Solis infusion pumps

## Reason for recall

The adapter input plug can become damaged or broken.  If the input plug is damaged, the metal contacts to the body of the AC adapter may be exposed or one or more of the AC mains prongs may separate from the input plug.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-0466-2025
- **Recalling firm:** Smiths Medical ASD, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-26
- **Report date:** 2024-11-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Minneapolis, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0466-2025

## Citation

> AI Analytics. FDA recall Z-0466-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-0466-2025. Source: US FDA. Licensed CC0.

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