FDA Device recall Z-0430-2024
ProCuity bed series, model number 3009, item number: 3009PX-LEX-450
- 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: 3009PX-LEX-450 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-0430-2024 |
| 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: 3009PX-LEX-450.
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): 07613327541236. Serial numbers: 2207000806 , 2101001244 , 2206000635…UDI-DI (GTIN): 07613327541236. Serial numbers: 2207000806 , 2101001244 , 2206000635 , 2206000628 , 2206000626 , 2206000483 , 2206000479 , 2206000412 , 2206000405 , 2206000401 , 2206000177 , 2205000560 , 2107001062 , 2107001046 , 2205000843 , 2205000841 , 2205000840 , 2205000836 , 2205000832 , 2208000197 , 2208000174 , 2208000156 , 2211002859 , 2205000935 , 2207001318 , 2207001289 , 2207001178 , 2207001163 , 2207001155 , 2207001114 , 2211000184 , 2211000209 , 2207001100 , 2207001097 , 2207001095 , 2207001 |
|---|
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-0430-2024%22
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