Medical devicesUpdated Jan 3, 2026HILL-ROM, INC.Official source

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

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    In plain language

    This recall involves Centrella Max and Pro+ Mattress Replacement System (MRS) Hospital Bed Mattresses sold in Canada. It's being recalled because of a sterility issue due to potential delamination of the top cover. Contact the manufacturer for more information.

    What to do

    • Stop using the product immediately.
    • Contact the manufacturer if you require additional information.

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    Affected products

    • Pro+ MRS Surface

      Model: P7924A03, P7924A04

      Lot: All lots distributed from March 1, 2022.

    • Pro+ MRS Surface For Hillrom 900 With X-Ray

      Model: P006800A01

      Lot: All lots distributed from March 1, 2022.

    • Centrella Pro+ Surface With X-Ray

      Model: P7923A01, P7923A02

      Lot: All produced after June 9, 2020.

    • Pro+ MRS Surface For VersaCare

      Model: P3255A02

      Lot: All lots distributed from March 1, 2022.

    • Pro+ MRS Surface With X-Ray

      Model: P7924A01, P7924A02

      Lot: All produced after June 9, 2020.

    • Centrella Max Surface

      Model: P7922A01, P7922A02

      Lot: All produced after June 9, 2020.

    • Centrella Pro+ Surface

      Model: P7923A03, P7923A04

      Lot: All lots distributed from March 1, 2022.

    • Pro+ MRS Surface For VersaCare With X-Ray

      Model: P3255A01

      Lot: All produced after June 9, 2020.

    Why this matters

    Sterility issue

    Do I have this product?

    This recall only applies to specific products. Follow the steps below to check.

    1. 1

      Check the product name

      Make sure your product name matches one of the affected products listed above.

    2. 2

      Check the lot number

      Lot numbers identify specific production batches.

      Affected lots: All lots distributed from March 1, 2022., All produced after June 9, 2020.

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: P006800A01, P3255A01, P3255A02, P7922A01, P7922A02, P7923A01, P7923A02, P7923A03, P7923A04, P7924A01, P7924A02, P7924A03, P7924A04

    If your product matches one or more of the details above, it may be affected by this recall.

    If your product does not match these details, it is not affected by this recall.

    When in doubt, always check the official notice.

    Want alerts if similar products are recalled in Canada?

    Frequently Asked Questions

    Why was this product recalled?

    Sterility issue

    What should consumers do?

    Stop using the product immediately. Contact the manufacturer if you require additional information.

    Where was the product sold?

    This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.

    Is there a health risk?

    Yes, there may be a health risk. Sterility issue

    When was this product recalled?

    This product was recalled on July 2, 2024.

    Is the HILL-ROM, INC. brand affected by this recall?

    Yes, HILL-ROM, INC. products are affected by this recall. This recall involves Centrella Max and Pro+ Mattress Replacement System (MRS) Hospital Bed Mattresses sold in Canada. It's being recalled because of a sterility issue due to potential delamination of the top cover. Contact the manufacturer for more information.