Power-PRO 2- A powered ambulance cot that consists of a platform — Class II medical device recall Z-2130-2023
Ongoing recall by Stryker Medical Division of Stryker Corporation, reported 2023-07-19, distributed nationwide. Base leg assembly may bend and result in difficulty engaging/disengaging from fastener, difficulty loading/unl
| Recall number | Z-2130-2023 |
|---|---|
| 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 | 2023-05-24 |
| Classified | 2023-07-12 |
| Reported by FDA | 2023-07-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CH, GB, NL |
| Quantity | 1,980 cots |
| UPC / GTIN / UDI-DI | 00650700000000, 07613327504460, 07613327559118, 07613327559125 |
| Serial numbers | 2112001485, 2112001488, 2112001489, 2112001490, 2112001491, 2112001492, 2112001493, 2112001494, 2112001495, 2112001496, 2112001501, 2112001503, 2112001504, 2112001508, 2112001509, 2112001510, 2112001511, 2112001512, 2112001513, 2112001514, 2112001515, 2112001516, 2112001517, 2112001518, 2112001519 and 475 more |
| Model numbers | 6507, 650700000000, 650705550001, 650705550002 |
Product
Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled, retractable X-frame that is designed to support and transport a maximum weight of 700 lb (318 kg). Model Number: 6507
Reason for recall
Base leg assembly may bend and result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty raising or lowering the cot, cot tip, or erratic or unintended motion.
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-2130-2023. 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.