Reported Nov 9, 2022 · Ongoing

Hillrom Centrella Hospital Bed with WatchCare Incontinence Management System, Product code/Part numbers: P7900B100193,…

Baxter Healthcare Corporation

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

  • Hillrom Centrella Hospital Bed with WatchCare Incontinence Management System
  • Product code/Part numbers

    74 of 74 codes

    • P7900B100193
    • P7900B100195
    • P7900B100230
    • P7900B100236
    • P7900B100239
    • P7900B100244
    • P7900B100256
    • P7900B100257
    • P7900B100259
    • P7900B100264
    • P7900B100268
    • P7900B100269
    • P7900B100292
    • P7900B100296
    • P7900B100302
    • P7900B100303
    • P7900B100304
    • P7900B100305
    • P7900B100312
    • P7900B100316
    • P7900B100318
    • P7900B100335
    • P7900B100341
    • P7900B100342
    • P7900B100354
    • P7900B100361
    • P7900B100368
    • P7900B100372
    • P7900B100381
    • P7900B100382
    • P7900B100384
    • P7900B100385
    • P7900B100387
    • P7900B100388
    • P7900B100392
    • P7900B100395
    • P7900B100396
    • P7900B100407
    • P7900B100408
    • P7900B100438
    • P7900B100441
    • P7900B1PL270
    • P7900B1PLT71
    • P7900B1SPL05
    • P7900B200193
    • P7900B200195
    • P7900B200230
    • P7900B200236
    • P7900B200264
    • P7900B200268
    • P7900B200292
    • P7900B200302
    • P7900B200318
    • P7900B200342
    • P7900B200361
    • P7900B200372
    • P7900B200381
    • P7900B200382
    • P7900B200392
    • P7900B200395
Lot codes and dates
  • UDI/DI 887761985162, all serial numbers
Amount recalled
6407 units

This recall covers 11 products

The agency filed one notice per product. You are reading one of them; the other 10 are below.

Why it was recalled

Stop using this product now

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).

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:51 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.