FDAFebruary 1, 2023device

Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement while loading/unloading or transport.

What to do

FDA enforcement status: Ongoing

Brands named

stryker medical divisionstrykerstryker medical

UPCs

07613327559118650705550001

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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