Power-PRO 2 — Class II medical device recall Z-0479-2023
Ongoing recall by Stryker Medical Division of Stryker Corporation, reported 2022-12-21, distributed nationwide. Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients s
| Recall number | Z-0479-2023 |
|---|---|
| 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 | 2022-11-11 |
| Classified | 2022-12-14 |
| Reported by FDA | 2022-12-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, GB, NL |
| UPC / GTIN / UDI-DI | 00650700000000, 07613327504460 |
| Serial numbers | 2112001485, 2112001488, 2112001489, 2112001490, 2112001491, 2112001492, 2112001493, 2112001494, 2112001495, 2112001496, 2112001501, 2112001503, 2112001504, 2112001508, 2112001509, 2112001511, 2112001512, 2112001513, 2112001514, 2112001515, 2112001516, 2112001517, 2112001518, 2112001519, 2112001520 and 349 more |
| Model numbers | 6507, 650705550001 |
Product
Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Reason for recall
Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.
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-0479-2023. 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.