[pending] Stryker MV3 bariatric bed, Part Number 5900000001
Pending LLM rewrite. Source: FDA_DEVICE Z-0918-2026.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Pending LLM scoring against the rubric.
Plain-English summary
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.
The recalled product
- Product
- Stryker MV3 bariatric bed, Part Number 5900000001
- Manufacturer
- Stryker Medical Division of Stryker Corporation
- Category
- Medical Device — Devices
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.
Related recalls
Same category
- ModeratePhilips Allura X-ray Systems Deaeration Hose Degradation Recall
FDA (Devices) · 2026-05-27
- HighMedtronic DLP Retrograde Cannula 13FR Model 94913L Recall
FDA (Devices) · 2026-05-27
- HighTangent Single Use Digital Catheter Recalled for Distal Shaft Fractures
FDA (Devices) · 2026-05-27
- HighMedtronic GUNDRY Retrograde Cannula vascular catheter sterile barrier breach
FDA (Devices) · 2026-05-27
- HighSwan-Ganz Jr Catheter models recalled due to lumen hub leakage
FDA (Devices) · 2026-05-27