Reported Dec 17, 2025 · Ongoing

Stryker Arise 1000EX mattress, Part Number 2236000000

Stryker Medical Division of Stryker Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Stryker Medical Division of Stryker Corporation · 3800 E Centre Ave · Portage, MI · 49002-5826

Is this the product you have?

    • Stryker Arise 1000EX mattress
    • Part Number 2236000000
Lot codes and dates
  • GTIN 00857268006608
  • Serial Numbers

    297 of 297 codes

    • 1000502893
    • 1000281054
    • 1000281055
    • 1000281056
    • 1000213521
    • 1000213522
    • 1000213529
    • 1000213530
    • 1000213531
    • 1000213532
    • 1000213533
    • 1000214321
    • 1000214331
    • 1000377179
    • 1000377180
    • 1000377181
    • 1000382290
    • 1000382291
    • 1000382292
    • 1000382293
    • 20090709143150
    • 1000537621
    • 1000537622
    • 1000481695
    • 1000481811
    • 1000502644
    • 1000502645
    • 1000469456
    • 1000469457
    • 1000469821
    • 1000469822
    • 1000065720
    • 1000066888
    • 1000502643
    • 1000502895
    • 1000508702
    • 1000510080
    • 1000510081
    • 1000510082
    • 1000510098
    • 1000183920
    • 1000183921
    • 1000184053
    • 1000451149
    • 1000451347
    • 1000485570
    • 1000232648
    • 1000232649
    • 1000232650
    • 1000232651
    • 1000232652
    • 1000512470
    • 1000514147
    • 1000510095
    • 1000510096
    • 1000482548
    • CU400-1983BA355214
    • 1000452867
    • 1000452869
    • 1000475796
Amount recalled
297 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:57 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.