Hillrom Hospital Bed Accessory — Class I medical device recall Z-0142-2023
Ongoing recall by Baxter Healthcare Corporation, reported 2022-11-09. Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including,
| Recall number | Z-0142-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-09-30 |
| Classified | 2022-10-31 |
| Reported by FDA | 2022-11-09 |
| Quantity | 814 units |
| UPC / GTIN / UDI-DI | 00887761984998 |
| Model numbers | P00697905 |
Product
Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Centrella Bed, Product Code/Part Number P00697905
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).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0142-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.