FDAAugust 14, 2017device

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

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

The hazard

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

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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