# FDA recall Z-0143-2023

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2022-09-30.

## Product

Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Progressa Bed, Product Code/Part Number P00697903.

## Reason for recall

Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scanner, fetal monitor/doppler, infusion pumps, and insulin pumps).

## Distribution

US

## Key facts

- **Recall number:** Z-0143-2023
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-09-30
- **Report date:** 2022-11-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0143-2023

## Citation

> AI Analytics. FDA recall Z-0143-2023. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-0143-2023. Source: US FDA. Licensed CC0.

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