FDA Device recall Z-0425-2024
ProCuity bed series, model number 3009, item number: 3009PX-L-100
- 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-L-100 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-0425-2024 |
| 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-L-100.
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): 07613327541168. Serial numbers: 2111000766 & 2107000368 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
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FDA Device · Class II · 2025-12-17 · Stryker Medical Division - ProCuity bed series, model number 3009, item number: 3009PX-ZM-600
FDA Device · Class II · 2023-12-13 · Stryker Medical Division - ProCuity bed series, model number 3009, item number: 3009PX-L-200
FDA Device · Class II · 2023-12-13 · Stryker Medical Division
All Stryker Medical Division recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0425-2024%22
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