# FDA recall Z-2420-2024

> **Smiths Medical ASD Inc.** · Class I · device recall initiated 2024-02-27.

## Product

CADD-Solis VIP ambulatory Infusion Pumps, Model 2110.  Indicated for the following uses:  Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a continuous rate of infusion, intermittent bolus, and/or with patient-controlled demand doses.

## Reason for recall

The CADD Solis VIP Ambulatory Infusion Pump is indicated for the following uses:  " For intravenous, intraarterial, subcutaneous, intraperitoneal, perineural, surgical site, epidural space, or subarachnoid space infusion.

## Distribution

Worldwide

## Key facts

- **Recall number:** Z-2420-2024
- **Recalling firm:** Smiths Medical ASD Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-27
- **Report date:** 2024-08-14

- **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-2420-2024

## Citation

> AI Analytics. FDA recall Z-2420-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2420-2024. Source: US FDA. Licensed CC0.

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