CLASS I ONGOING Device recall · Reported 9 Nov 2022 · FDA Enforcement Report

Hillrom Hospital Bed Accessory recalled by Baxter Healthcare

Baxter Healthcare is recalling Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Progressa. The recall was initiated on 30 Sep 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUDI/DI 00887761998889, all serial numbers

Quantity recalled1137 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0143-2023
FDA event ID: 90865
Recalling firm: Baxter Healthcare, Deerfield, IL
Classification: Class I
Status: Ongoing
Recall initiated: 30 Sep 2022
FDA classified: 31 Oct 2022
Reported: 9 Nov 2022
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Wheelchairs, Beds & Lifts

Timeline

30 Sep 2022	Recall initiated by company
31 Oct 2022	Classified by FDA	+31 days
9 Nov 2022	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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).

Product as listed by the FDA

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

Where it was distributed

Questions about this recall

Why was it recalled?

Which lots are affected?

UDI/DI 00887761998889, all serial numbers

Where was it sold?

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 90865

Reported	Class	Recall	Company	Reason	Where
9 Nov 2022	CLASS I	Hillrom Hospital Bed Accessory recalled by Baxter Healthcare	Baxter Healthcare	Other	IL
9 Nov 2022	CLASS I	Hillrom Centrella Hospital Bed recalled by Baxter Healthcare	Baxter Healthcare	Other	IL
9 Nov 2022	CLASS I	Hillrom Hospital Bed Accessory recalled by Baxter Healthcare	Baxter Healthcare	Other	IL
9 Nov 2022	CLASS I	Hillrom Hospital Bed Accessory recalled by Baxter Healthcare	Baxter Healthcare	Other	IL

More recalls from Baxter Healthcare

All 570

Reported	Class	Recall	Company	Reason	Where
16 Sep 2026Drug	CLASS I	Dextrose Injection, USP, 70 % recalled by Baxter Healthcare	Baxter Healthcare	Particulate Matter	Nationwide
9 Sep 2026Drug	CLASS I	0.9% Sodium Chloride Injection USP, Viaflex recalledSodium Chloride	Baxter Healthcare	Particulate Matter	IL
9 Sep 2026Device	CLASS II	Baxter Novum IQ Syringe Pump, Loaner recalled by Baxter Healthcare	Baxter Healthcare	Device Malfunction	Nationwide
9 Sep 2026Device	CLASS II	Baxter Novum IQ Syringe Pump recalled by Baxter Healthcare	Baxter Healthcare	Device Malfunction	Nationwide
9 Sep 2026Drug	CLASS II	Clindamycin Phosphate in 0.9% Sodium Chloride Injection recalledClindamycin Phosphate	Baxter Healthcare	Manufacturing (CGMP) Deviations	Nationwide

Other Wheelchairs, Beds & Lifts recalls

All 172

Reported	Class	Recall	Company	Reason	Where
12 Aug 2026Device	CLASS II	Quantum Rehab Quantum 4Front 2HD recalled by Pride Mobility Products	Pride Mobility Products	Device Malfunction	Nationwide
12 Aug 2026Device	CLASS II	Quantum Rehab Q6 Edge 2.0 (ilevel) recalled by Pride Mobility Products	Pride Mobility Products	Device Malfunction	Nationwide
12 Aug 2026Device	CLASS II	Quantum Rehab Q6 Edge recalled by Pride Mobility Products	Pride Mobility Products	Device Malfunction	Nationwide
12 Aug 2026Device	CLASS II	Quantum rehab Q6 Edge recalled by Pride Mobility Products	Pride Mobility Products	Device Malfunction	Nationwide
12 Aug 2026Device	CLASS II	Quantum Rehab Q6 Edge recalled by Pride Mobility Products	Pride Mobility Products	Device Malfunction	Nationwide