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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