Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ReWalk Personal 6.0. Catalog number: 50-20-0004. Recalled by Argo Medical Technologies Ltd Due to Firm received complaints for ReWalk Personal 6.0 of...
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. Catalog number: 50-20-0004.
Quantity: 127
Why Was This Recalled?
Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula.
Where Was This Sold?
US and foreign.
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