Baxter recalls Hillrom WatchCare Incontinence Management System for VersaCare Bed Rev. K due to potential radio frequency interference with medical devices like infusion pumps and fetal monitors.
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).
Baxter is recalling Hillrom's WatchCare Incontinence Management System for Vers: Care Bed Rev. K because it may emit radio frequencies that interfere with medical devices. This could affect critical equipment like infusion pumps and fetal monitors if used in healthcare settings.
The WatchCare device may emit radio frequencies that interfere with other medical devices. This could cause malfunctions in critical equipment such as infusion pumps, fetal monitors, or insulin pumps if they are in close proximity.
Healthcare facilities using the VersaCare Bed Rev. K with WatchCare system are most at risk. Patients on medical devices like infusion pumps or fetal monitors could be affected if the system is in use.
Check for the product code/part number P00697902, UDI/DI 887761998872, or any serial numbers on the device. The system is designed for VersaCare Bed Rev. K hospital beds.
Look for the product code/part number P00697902, UDI/DI 887761998872, or serial numbers on the device.
The recall states that radio frequency emissions may interfere with medical devices, so it's recommended to check if you have the affected model and follow the action steps.
The recall does not specify a remedy, so you should check the product details and contact Baxter Healthcare if you have the affected model.
The recall does not mention a risk of serious injury, only potential interference with medical devices.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0144-2023 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-0144-2023 from Baxter Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
