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Argo Medical Technologies Ltd recalls ReWalk Personal 6.0. Catalog number: 50-20-0004.
Recalled March 21, 2018 · FDA recall Z-0944-2018 · Argo Medical Technologies
Hazard
Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula. · FDA Class II
Units
127
Sold at
US and foreign.
Description
Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula.
Product
ReWalk Personal 6.0. Catalog number: 50-20-0004.
Manufacturer(s)
Argo Medical Technologies Ltd
Made in
Israel
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →