Recall Z-1935-2020— Stryker Medical Division of Stryker Corporation
Class II · Terminated
Class II FDA medical device recall by Stryker Medical Division of Stryker Corporation, initiated 2020-04-07, terminated 2021-01-22. FDA's recall record names no specific 510(k) clearance for this event. Product: Stryker Power-PRO TL cot-powered ambulance cot Model Number 6550 - Product Usage: is a powered wheeled stretcher that is intended to support and transport the entire body of a traumatized, ambulatory or non-ambulatory human patient (includes infants and adults).. Reason: Ambulance Cots may not meet crash test standard BS EN 1789.
- Recalling firm
- Stryker Medical Division of Stryker Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2020-04-07
- Terminated
- 2021-01-22
- Firm location
- Portage, MI, United States
Product description
Stryker Power-PRO TL cot-powered ambulance cot Model Number 6550 - Product Usage: is a powered wheeled stretcher that is intended to support and transport the entire body of a traumatized, ambulatory or non-ambulatory human patient (includes infants and adults).
Reason for recall
Ambulance Cots may not meet crash test standard BS EN 1789
Data sourced from openFDA. This site is unofficial and independent of the FDA.