Recall Z-2130-2023— Stryker Medical Division of Stryker Corporation
Class II · Ongoing
Class II FDA medical device recall by Stryker Medical Division of Stryker Corporation, initiated 2023-05-24. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Stryker Medical Division of Stryker Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-05-24
- Firm location
- Portage, MI, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.