Health product recall

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

Brand(s)
Last updated

Summary

Product
Centrella Max and Pro+ Mattress Replacement System (MRS) Hospital Bed Mattresses
Issue
Medical devices - Sterility
What to do

Contact the manufacturer if you require additional information. 

Affected products

Affected products

Lot or serial number

Model or catalog number

Pro+ MRS Surface

All lots distributed from March 1, 2022.

P7924A03
P7924A04

Pro+ MRS Surface For Hillrom 900 With X-Ray

All lots distributed from March 1, 2022.

P006800A01

Centrella Pro+ Surface With X-Ray

All produced after June 9, 2020.

P7923A02
P7923A01

Pro+ MRS Surface For VersaCare

All lots distributed from March 1, 2022.

P3255A02

Pro+ MRS Surface With X-Ray

All produced after June 9, 2020.

P7924A02
P7924A01

Centrella Max Surface

All produced after June 9, 2020.

P7922A01
P7922A02

Centrella Pro+ Surface

All lots distributed from March 1, 2022.

P7923A04
P7923A03

Pro+ MRS Surface For VersaCare With X-Ray

All produced after June 9, 2020.

P3255A01

Issue

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

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Hill-Rom, Inc.

1069 State Route 46 East, Batesville, Indiana, United States, 47006-9167

Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-75768

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