Recall Z-0479-2023— Stryker Medical Division of Stryker Corporation
Class II · Ongoing
Class II FDA medical device recall by Stryker Medical Division of Stryker Corporation, initiated 2022-11-11. FDA's recall record names no specific 510(k) clearance for this event. Product: Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International). Reason: 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..
- Recalling firm
- Stryker Medical Division of Stryker Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-11-11
- Firm location
- Portage, MI, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.