FDA Device recall Z-2130-2023
Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled, retractable X-frame that is d…
- FDA Device
- Class II
- ongoing
- Published 2023-07-19
On 2023-07-19 the FDA classified a Class II recall of Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled, retractable X-frame that is d… by Stryker Medical Division, citing 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 ti….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2130-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-05-24 |
| Published | 2023-07-19 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Stryker Medical Division |
| Distribution | US |
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
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.
Identifiers
| code_info | Model: 650700000000 UDI-DI: 07613327504460; Model: 650705550001 UDI-DI: 07613327559118; Model: 650705550002…Model: 650700000000 UDI-DI: 07613327504460; Model: 650705550001 UDI-DI: 07613327559118; Model: 650705550002 UDI-DI: 07613327559125; Cots shipped between February 11, 2022 and February 1, 2023 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 2112001520 2112001521 2112001522 2112001523 2112001524 |
|---|
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-2130-2023%22
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