Medical device recalls Moderate risk

Stryker Medical Division of Stryker product recalled over injury risk

Recall date
April 7, 2020
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Stryker Medical Division of Stryker Corporation recalls Stryker Power-PRO TL cot-powered ambulance cot Model Number 6550 - Product Usage: is a powered wheeled stretcher that i…
Recall number
Z-1935-2020
FDA classification
Class II
Brand / firm
Stryker Medical Division of Stryker Corporation
Sold / distributed
Foreign: UK

Why it was recalled

Ambulance Cots may not meet crash test standard BS EN 1789

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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).

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