Argo Medical Technologies Ltd: Medical Device Recall in 2018 - (Recall #: Z-0944-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 14, 2017

Date Posted: March 21, 2018

Recall Number: Z-0944-2018

Event ID: 79186

Reason for Recall:

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

Status: Terminated

Product Quantity: 127

Code Information:

Date range of Distribution: 09/01/2015 to 09/06/2017.

Distribution Pattern:

US and foreign.

Voluntary or Mandated:

Voluntary: Firm initiated