Recall of Hillrom Centrella Hospital Beds with WatchCare Incontinence Management System 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).
Hillrom is recalling hospital beds with the WatchCare Incontinence Management System because radio waves from the device could interfere with medical equipment. This poses a risk to patients using devices like infusion pumps or fetal monitors.
The WatchCare device emits radio frequency signals that might interfere with other medical devices such as infusion pumps, insulin pumps, and fetal monitors. This could cause inaccurate readings or malfunctions in critical equipment.
Hospital users and patients who have the specific Hillrom Centrella beds with the WatchCare system are most at risk, particularly those with medical devices that could be affected by radio frequency emissions.
Check for the product codes listed in the recall: P7900B100193 through P7900B200485, or the UDI/DI number 887761985162. These are specific to the Hillrom Centrella Hospital Bed with WatchCare system.
Identify if your bed has any of the listed product codes (P7900B100193 through P7900B200485) or the UDI/DI number 887761985162.
Infusion pumps, insulin pumps, fetal monitors, and bladder scanners could be affected by radio frequency emissions from the WatchCare device.
Check the product codes listed in the recall: P7900B100193 through P7900B200485, or the UDI/DI number 887761985162.
No action is needed if your bed does not have the listed product codes or UDI/DI number.
We’ve drafted a message you can send Hillrom to request your refund or repair — edit it as you like.
Subject: Recall Z-0141-2023 — Hillrom Hillrom Hello, I own a Hillrom that is covered by recall Z-0141-2023 from Hillrom. 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.
