FDA Device recall Z-0435-2024
ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600
- FDA Device
- Class II
- ongoing
- Published 2023-12-13
On 2023-12-13 the FDA classified a Class II recall of ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600 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-0435-2024 |
| 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
ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600.
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): 07613327541328. Serial numbers: 2209001834, 2209001941 , 2209001939 , 22110…UDI-DI (GTIN): 07613327541328. Serial numbers: 2209001834, 2209001941 , 2209001939 , 2211002329 , 2211002319 , 2211000556 , 2205000776 , 2106000019 , 2202002062 , 2106001528 , 2106001515 , 2209001539 , 2203000249 , 2106002482 , 2202001091 , 2203000298 , 2203000098 , 2108000232 , 2208000679 , 2110000200 , 2106002061 , 2106002051 , 2106001697 , 2211004469 , 2211004828 , 2206001229 , 2206001234 , 2211004824 , 2106001589 , 2209002761 , 2209002730 , 2209002674 , 2111000113 , 2111000111 , 2208001113 |
|---|
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-0435-2024%22
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