Stryker Arise 1000EX mattress, Part Number 2236000000 recallZ-0919-2026 · Stryker Medical Division of Stryker Corporation · initiated Oct 31, 2025

Open, Classified

Is my device affected?

Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
If yours is listed, follow the instructions from Stryker Medical Division of Stryker Corporation or your healthcare provider. The company's action is summarized under what the company is doing.
Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

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.

FDA root cause category: Release of Material/Component prior to receiving test results

What the company is doing

Stryker issued an URGENT: VOLUNTARY MEDICAL DEVICE SAFETY notice to its sales representatives on 11/13/2025 for hand delivery to its consignees on 11/14/2025. The notice explained the issue, potential hazard, and requested the following: "Actions needed: 1. Locate the MV3 and Arise 1000EX devices that have been shipped to your facility. Serial numbers are provided on the enclosed business reply form. 2. If an MV3 is being used together with an Arise 1000EX mattress, Stryker recommends the use to be discontinued upon receipt of this notification. 3. Complete the enclosed business reply form to confirm receipt of this notification. 4. Return your completed business reply form to Stryker by fax +1 269 488 8691 or email [email protected]. 5. For those requesting a replacement of a compatible mattress, Stryker will contact you upon receipt of your Business Reply Form for next steps. 6. If you have loaned or sold any of the products listed in this letter, please forward a copy of this notice to the new users and advise us of their new location." For questions or concerns, contact Customer Service at +1 800 327 0770, Option 1 for Customer Support, Monday through Friday from 8:00 a.m. to 7:00 p.m. ET.

Recall details

Recall number: Z-0919-2026
Status: Open, Classified
Initiated by the company: Oct 31, 2025
Posted by the FDA: Dec 11, 2025
Recalling firm: Stryker Medical Division of Stryker Corporation
Quantity: 297 units
Product code: FNM
Distribution: US, nationwide

Product description

Stryker Arise 1000EX mattress, Part Number 2236000000

Code information (models, lots, serial numbers)

Show the full code information (4k characters)

GTIN 00857268006608, Serial Numbers: 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, 1000475797, 1000475867, 1000475868, 1000485537, 1000485571, 1000485538, 1000471627, 1000471860, 3100000471, 3100000874, 1000486159, 1000495054, 1000495055, 1000484745, 1000484746, 1000484747, 1000456813, 1000467673, 1000483228, 1000483229, 1000483465, 1000483466, 1000483467, 1000483468, 1000468975, 1000468976, 1000483230, 1000514148, 1000514149, 1000455365, 1000455367, 1000456815, 1000053839, 1000181244, 1000482317, 1000482318, 1000482319, 1000276077, 1000393550, 1000481813, 1000370748, 1000372689, 1000372690, 1000372691, 1000372692, 1000372693, 1000372694, 1000372695, CU400-1375, CU400-1447, 1000451346, 1000361096, 1000361097, 1000422407, 1000422427, 1000422428, 1000484748, 1000502891, 1000502892, 1000535388, 1000160222, 1000500377, 1000500378, 1000500654, 1000504503, 1000504504, 1000504505, 1000055394, 1000260702, 1000260703, 1000260704, 1000454956, 1000435830, 1000435831, 1000514150, 1000446907, 1000446908, 1000335539, 1000411780, 1000417224, 1000007185, 1000007187, 1000007188, 1000007189, 1000046411, 1000046735, 1000048762, 1000512471, 1000512474, 1000514151, 1000514152, 1000514153, 1000514154, 1000514155, 1000521760, MX110241, MX110245, 1000436370, 1000436372, 1000482545, 1000482546, 1000482547, 1000454955, 1000454957, 1000455328, 1000455329, 1000387606, 1000387836, 1000480162, 1000373921, 1000373922, 1000373923, 1000373924, 1000389360, 1000389361, 1000500655, 1000431889, 1000431891, 1000431892, 1000431893, 1000431894, 1000446831, 1000481812, 1000476944, 1000476945, 1000479698, 1000479699, 1000479700, 1000480160, 1000480161, 1000483231, 1000483994, 1000483995, 1000483996, 1000483997, 3100000278, 1000354259, 1000413269, 1000413270, 1000413271, 1000413272, 1000417222, 1000417223, 1000418007, 1000418008, 1000418009, 1000422044, 1000422045, 1000422046, 1000422047, 1000422098, 1000422099, 1000422100, 1000422101, 1000422102, 1000422103, 1000422104, 1000422105, 1000422106, 1000422107, 1000422108, 1000422109, 1000422404, 1000422405, 1000422406, 1000422429, 1000422430, 1000422431, 1000422432, 1000422433, 1000422434, 1000426512, 1000426513, 1000426514, 1000426515, 1000426516, 1000426517, 1000426518, 1000426519, 1000426795, 1000426796, 1000426797, 1000426798, 1000426799, 1000426800, 1000426801, 1000426802, 1000427341, 1000427342, 1000427343, 1000427344, 1000427345, 1000427346, 1000427347, 1000427348, 1000427349, 1000427350, 1000427351, 1000427352, 1000427353, 1000427354, 1000427355, 1000427356, 1000427634, 1000427635, 1000427636, 1000427637, 1000427638, 1000427639, 1000427640, 1000427641, 1000427701, 1000427702, 1000427703, 1000427704, 1000427705, 1000427706, 1000427707, 1000427708, 1000428096, 1000428097, 1000428098, 1000428099, 1000428100, 1000428101, 1000428102, 1000428103, 1000428297, 1000232647, 1000531402, 1000531401, 1000531403, 1000524879, 1000524877, 1000524878, 1000531400, 1000524880.

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

Arise 1000 EX AREXLAL-CU
Joerns Healthcare, LLC · Mattress, Air Flotation, Alternating Pressure
1 recall0 reports

Other products in the same recall event

The FDA groups related products into one recall event (event 97953).

Z-0918-2026 · Open, Classified
Stryker MV3 bariatric bed, Part Number 5900000001

Sources and updates

Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.

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