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Centrella Max and Pro+ Mattress Replacement System (MRS) Hospital Bed… — recall 75768

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

As described by Health Canada — Medical Devices: Centrella Max and Pro+ Mattress Replacement System (MRS) Hospital Bed Mattresses

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
75768
Date of alert
2024-07-02
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
General hospital and personal use
Product type
Medical devices
Reported risk: 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
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/centrella-max-and-pro-mattress

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