FDA Device recall Z-0142-2023
Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Centrella Bed, Product Code/Part Number P00697905
- FDA Device
- Class I
- ongoing
- Published 2022-11-09
On 2022-11-09 the FDA classified a Class I recall of Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Centrella Bed, Product Code/Part Number P00697905 by Baxter Healthcare, citing radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scanner, fetal monitor/….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0142-2023 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2022-09-30 |
| Published | 2022-11-09 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | n/a |
Product
Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Centrella Bed, Product Code/Part Number P00697905
Reason
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).
Identifiers
| code_info | UDI/DI 887761984998, all serial numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0142-2023%22
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