FDA Device recall Z-0424-2024
ProCuity bed series, model number 3009, item number: 300900000000
- FDA Device
- Class II
- ongoing
- Published 2023-12-13
On 2023-12-13 the FDA classified a Class II recall of ProCuity bed series, model number 3009, item number: 300900000000 by Stryker Medical Division, citing patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0424-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-08-30 |
| Published | 2023-12-13 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Stryker Medical Division |
| Distribution | US |
Product
ProCuity bed series, model number 3009, item number: 300900000000,
Reason
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Identifiers
| code_info | UDI-DI (GTIN): 07613327512656. Serial numbers: 2207000698, 2207000676, 2207000619, 2206001100, 2206001090, 2206001089,…UDI-DI (GTIN): 07613327512656. Serial numbers: 2207000698, 2207000676, 2207000619, 2206001100, 2206001090, 2206001089, 2206001086, 2206001084, 2208001745, 2208001734, 2208001725, 2208001724, 2208000397, 2208000394, 2208000032, 2209002157, 2209002158, 2209002165, 2210000711 , 2210000721 , 2210000723 , 2111000494 , 2206001248 , 2206001250 , 2206001265 , 2206001273 , 2206001317 , 2207000023 , 2207000078 , 2207000303 , 2207000307 , 2207000342 , 2207000350 , 2207000353 , 2207000358 , 2110002355 , 2108002264 , 2209000269 , 2106002756 , 2103001270 , 2109000898 , 2109001004 , 2108001784 , 2107001856 , 2208000874 , 2208000 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0424-2024%22
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