Bariatric hospital beds recalled because they are not tested with certain mattresses
Stryker is recalling 294 MV3 bariatric beds because they and Arise 1000EX mattresses have been sold in close proximity, and the two products have not been tested for compatibility.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: Scored 2 because the record cites an untested product combination with no stated defect, consequence or reported harm.
Plain-English summary
The Stryker MV3 bariatric bed, part number 5900000001, is being recalled by the Stryker Medical Division of Stryker Corporation.
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. The firm states these products have not been tested for compatibility and are not designed to be used together, and that the combination of both is not recommended by Stryker.
The recall covers 294 units carrying GTIN 07613327419221, with affected serial numbers listed in the enforcement record. Distribution was nationwide in the United States. The FDA has classified the action as Class II.
The record describes an untested product pairing rather than a defect in either item, and states no injuries. Facilities should follow Stryker's instructions.
The recalled product
- Product
- Stryker MV3 bariatric bed, Part Number 5900000001
- Manufacturer
- Stryker Medical Division of Stryker Corporation
- Category
- Medical Device — Hospital bed
- Affected units
- 294
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- GTIN 07613327419221. Serial Numbers: 2025013200138
- 2025013200139
- 2022013200001
- 2022013200002
- 2022013200003
- 2021013200096
- 2021013200098
- 2021013200099
- 2021013200102
- 2021013200114
- 2023013200036
- 2023013200037
- 2023013200038
- 2023013200039
- 2023013200040
- 2023013200041
- 2023013200042
- 2025013200200
- 2025013200201
- 2024013200239
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Stryker Medical Division of Stryker Corporation under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
Same manufacturer · Stryker Medical Division of Stryker Corporation
See all →- ModerateStryker Cub pediatric cribs sold in USA missing two warning labels
FDA (Devices) · 2026-03-25
- ModerateHospital mattresses recalled because they are not tested with certain beds
FDA (Devices) · 2025-12-17
- HighProCurity patient beds recalled for electrical safety testing defects
FDA (Devices) · 2023-12-13
- HighProCuity Hospital Patient Beds Recalled for Missing Electrical Safety Testing
FDA (Devices) · 2023-12-13
- HighProCuity Hospital Beds: Missing electrical safety tests pose burn and shock risk
FDA (Devices) · 2023-12-13