FDAFebruary 28, 2020device

ReWalk Personal 6.0, ReWalk Personal 5.0 and ReWalk R Systems orthotically fits to the lower limbs and part of the upper body and is intended to enable individuals with spinal cord injury at levels T7 to L5 to perform ambulatory functions.

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

The hazard

ReWalk Robotics received two complaints (one in the US; one in the Germany), which alleged that the ReWalk device waistpack (which is the location of the Li-Ion battery packs) caught fire while being charged.

What to do

FDA enforcement status: Terminated

Brands named

argo medical technologiesargoargo medical

Recall history

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

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