Reported Jul 27, 2022 · Ongoing

Hill-Rom Centrella Pro+ 36" Surface mattress, REF P7923A03.

Baxter Healthcare Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

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?

    • Hill-Rom Centrella Pro+ 36" Surface mattress
    • REF P7923A03
Lot codes and dates
  • UDI 00887761977921
  • Serial numbers

    70 of 70 codes

    • W217BP4016
    • W217BP4039
    • W217BP4040
    • W228BP4177
    • W228BP4179
    • W228BP4180
    • W228BP4189
    • W228BP4190
    • W228BP4193
    • W228BP4194
    • W228BP4195
    • W228BP4198
    • W228BP4199
    • W228BP4201
    • W217BP4014
    • W217BP4015
    • W217BP4018
    • W217BP4019
    • W217BP4024
    • W217BP4025
    • W217BP4026
    • W217BP4027
    • W217BP4037
    • W217BP4038
    • W228BP4173
    • W228BP4174
    • W228BP4175
    • W228BP4185
    • W228BP4186
    • W228BP4188
    • W228BP4196
    • W228BP4200
    • W217BP4017
    • W217BP4020
    • W217BP4021
    • W217BP4022
    • W217BP4023
    • W217BP4028
    • W217BP4029
    • W217BP4030
    • W217BP4031
    • W217BP4032
    • W217BP4033
    • W217BP4034
    • W217BP4035
    • W217BP4036
    • W228BP4183
    • W228BP4184
    • W228BP4191
    • X012BP7192
    • X012BP7193
    • X012BP7194
    • X012BP7195
    • X012BP7198
    • X012BP7199
    • X012BP7202
    • X012BP7203
    • X012BP7204
    • X012BP7205
    • X012BP7206
Amount recalled
70 mattresses

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

Why it was recalled

The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in an increased patient risk of pressure ulcer development.

This product could cause temporary or reversible health problems — stop using it.

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.

Free recall alerts

Get alerted about new Baxter Healthcare Corporation recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:20 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.