Stryker recalls certain Arise 1000EX mattresses (Part Number 2236000000) sold near MV3 beds due to untested compatibility. These products are not designed to be used together.
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.
Stryker is recalling specific Arise 1000EX mattresses because they were sold in close proximity to MV3 beds without being tested for compatibility. Using these products together could lead to improper function or safety issues.
The mattresses and beds were sold without being tested for compatibility. Stryker states they are not designed to be used together, which could cause improper function or safety issues if used together.
People who own the recalled Arise 1000EX mattress (Part Number 2236000000) or MV3 beds that were sold together. Those using these products together are most at risk.
Check for the Part Number 2236000000 on the mattress or the Serial Numbers listed in the recall notice. These items were sold in close proximity to MV3 beds.
Verify if your mattress has the Part Number 2236000000 or the listed Serial Numbers.
Stryker issued this recall because the mattress and MV3 beds were sold without being tested for compatibility, and they are not designed to be used together.
The recall does not require stopping use; it only advises against using the mattress with MV3 beds together.
The recall does not specify a remedy, so you can continue using it unless you are using it with an MV3 bed.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0919-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0919-2026 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
