ProCuity bed series — Class II medical device recall Z-0431-2024
Ongoing recall by Stryker Medical Division of Stryker Corporation, reported 2023-12-13, distributed nationwide. Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical
| Recall number | Z-0431-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Medical Division of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2023-08-30 |
| Classified | 2023-12-01 |
| Reported by FDA | 2023-12-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CH, CL, CN, ES, MX, PL |
| UPC / GTIN / UDI-DI | 07613327541250 |
| Serial numbers | 2110001715 |
| Model numbers | 3009, 3009PX-Z-450 |
Product
ProCuity bed series, model number 3009, item number: 3009PX-Z-450.
Reason for recall
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0431-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.