Reported Jun 26, 2024 · Ongoing

Centrella Max - The Centrella Smart+ Bed is intended for use in healthcare environments as a patient support system to…

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?

18 of 18 products

Products covered by this recall
Model / numberProduct as published
P7922A01Centrella Max - The Centrella Smart+ Bed is intended for use in healthcare environments as a patient support system to prevent and/or treat pressure injuries.Multiple model numbers of Centrella Max mattresses and pro+ mattresses. (1) Centrella Max Surface
P7922A02(2) Centrella Max Surface
P7922A03(3) Centrella Max Surface with X-Ray
P7922ARENT01(4) Centrella Max,Narrow, Rental
P7923A01(5) Centrella Pro+ 36" Surface with X-Ray
P7923A02(6) Centrella Pro+ 40" Surface with X-Ray
P7923A03(7) Centrella Pro+36" Surface
P7923A04(8) Centrella Pro+ 40" Surface
P006800A01(9) Pro+ MRS Surface for Hillrom 900 with X-Ray
P006800A03(10) 80" MRS with X-Ray AU/NZ
P3255A01(11) Pro+ MRS Surface for Versacare with X-Ray
P3255A02(12) Pro+ MRS Surface for Versacare
P3255ARENT01(13) Pro + MRS Surface for Versacare with X-Ray
P7924A01(14) Pro+ 36"MRS Surface with X-Ray
P7924A02(15) Pro+ 40" MRS Surface with X-Ray
P7924A03(16) Pro+ 36" MRS Surface
P7924A04(17) Pro+ 40" MRS Surface
P7924ARENT01.(18) Pro+ 36" MRS Rental Surface with X-Ray
Amount recalled
38,136 mattress units and 20,187 service part units

Where it was sold

  • Nationwide

Why it was recalled

There is a potential for the top cover of the hospital bed mattress to delaminate as a result of improper cleaning and lack of adequate details on the appropriate use of cleaning agents containing bleach.

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

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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, 4:56 PM UTC

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