Argo Medical Technologies Recalls

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.

Class I - Dangerous

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.

Feb 28, 2020 Infusion Pumps Nationwide View Details →

ReWalk Personal 6.0. Catalog number: 50-20-0004.

Class I - Dangerous

Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula.

Aug 14, 2017 Other Medical Devices View Details →