# FDA recall Z-1662-2025

> **Smiths Medical ASD, Inc.** · Class I · device recall initiated 2025-04-10.

## Product

CADD Solis HSPCA Pump

## Reason for recall

Pumps may experience Wireless Connection Modules intermittent connection alarms, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-1662-2025
- **Recalling firm:** Smiths Medical ASD, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-10
- **Report date:** 2025-05-14

- **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-1662-2025

## Citation

> AI Analytics. FDA recall Z-1662-2025. Retrieved 2026-09-27 from https://api.ai-analytics.org/recall/Z-1662-2025. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*