Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ReWalk Personal 6.0 Recalled by Argo Medical Technologies Ltd Due to ReWalk Robotics received two complaints (one in the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Argo Medical Technologies Ltd directly.
Affected Products
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.
Quantity: 350 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Argo Medical Technologies Ltd
Argo Medical Technologies Ltd has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report