FDA Device recall Z-0918-2026
Stryker MV3 bariatric bed, Part Number 5900000001
- FDA Device
- Class II
- ongoing
- Published 2025-12-17
On 2025-12-17 the FDA classified a Class II recall of Stryker MV3 bariatric bed, Part Number 5900000001 by Stryker Medical Division, citing 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 inte….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0918-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-10-31 |
| Published | 2025-12-17 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Stryker Medical Division |
| Distribution | US |
Product
Stryker MV3 bariatric bed, Part Number 5900000001
Reason
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.
Identifiers
| code_info | GTIN 07613327419221. Serial Numbers: 2025013200138, 2025013200139, 2022013200001, 2022013200002, 2022013200003, 202101…GTIN 07613327419221. Serial Numbers: 2025013200138, 2025013200139, 2022013200001, 2022013200002, 2022013200003, 2021013200096, 2021013200098, 2021013200099, 2021013200102, 2021013200114, 2023013200036, 2023013200037, 2023013200038, 2023013200039, 2023013200040, 2023013200041, 2023013200042, 2025013200200, 2025013200201, 2024013200239, 2024013200240, 2025013200041, 2025013200042, 2024013200264, 2024013200265, 2024013200266, 2024013200267, 2025013200043, 2025013200156, 2025013200157, 2025013200158, 2025013200159, 2020013200136, 2020013200137, 2021013200017, 2025013200172, 2024013200156, 2024013200157, 2020013200103, 2021013200079, 2021013200080, 2021013200087, 2021013200089, 2021013200091, 2021013200092, 2021013200093, 2021013200218, 2021013200219, 2021013200247, 2021013200249, 2025013200084, 2025013200087, 2025013200088, 2025013200089, 2025013200090, 2025013200091, 2025013200160, 2025013200161, 2025013200085, 2025013200086, 2022013200178, 2024013200286, 2024013200188, 2024013200189, 20 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0918-2026%22
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