# FDA recall Z-1682-2025

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

## Product

CADD Solis VIP Ambulatory Infusion Pump Models:    1) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL  MODE, 1/EA, Model Number: 21-2127-0105-01;     2) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, PHARMGUARD  ENABLED, 1/EA, Model Number: 21-2120-0105-01;     3) PUMP KIT, CADD-SOLIS VIP, MDL  2120, NA ENGLISH     1/EA, Model Number: 21-2120-0103-01;     4) PUMP, CADD-SOLIS VIP, MDL  2120, ENGLISH 1/EA, Model Number: 21-2120-0102-51;     5) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, PHARMGUARD  ENABLED    1/EA, Model Number: 21-2120-0104-01;     6) PUMP KIT, CADD-SOLIS VIP, MDL  2120, CE GLOBAL ENGLISH     1/EA, Model Number: 21-2120-0103-51;    7) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL MODE     1/EA, Model Number: 21-2127-0104-01;   8) PUMP KIT, CADD-SOLIS VIP, MDL 2120, TRIAL/LOANER, NA ENGLISH, PHARMGUARD, 1/EA, Model Number: 21-2120-0105-00;    9) PUMP, CADD-SOLIS VIP, MDL 2120, TRIAL/LOANER CE GLOBAL  ENGLISH    1/EA, Model Number: 21-2120-0103-78;   

## Reason for recall

There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-1682-2025
- **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-1682-2025

## Citation

> AI Analytics. FDA recall Z-1682-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1682-2025. Source: US FDA. Licensed CC0.

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