Official recall record

Centrella Max and Pro+ Mattress Replacement System (MRS) Hospital Bed Mattresses

Health Canada — Medical Devices · 2024-07-02 · CanadaType II

Issuing authority: Health Canada — Medical Devices
Published: 2024-07-02
Country of alert: Canada
Alert level: Type II
Alert type: recall

What the authority reported

Baxter Corporation is issuing a correction for the Centrella Max and Pro+ Mattress Replacement System (MRS) Hospital Bed Mattresses due to the potential for the top cover to delaminate. Contributing causes of delamination include improper cleaning of the product (i.e., excessive use of cleaning agents containing bleach) and a lack of adequate details on the appropriate use of cleaning agents containing bleach in the product instructions for use (IFU). Recall Start Date: May 13, 2024

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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