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Incident · Injury

ReWalk (now Lifeward) Personal 6.0: lateral tibial plateau fracture in a new user (FDA MAUDE)

An FDA MAUDE injury report describes a new user of the ReWalk Personal 6.0 powered exoskeleton sustaining a lateral tibial plateau fracture. ReWalk Robotics rebranded to Lifeward in 2024. Distinct from the 2017 ReWalk tibia/fibula recall (a recall, not a MAUDE report). Source: FDA MAUDE MDR key 10050473, accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE.

Occurred 2019-12-18 · Lifeward

Track ReWalk (now Lifeward) Personal 6.0: lateral tibial plateau fracture in a new user (FDA MAUDE)

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What happened in ReWalk (now Lifeward) Personal 6.0: lateral tibial plateau fracture in a new user (FDA MAUDE)?
An FDA MAUDE injury report describes a new user of the ReWalk Personal 6.0 powered exoskeleton sustaining a lateral tibial plateau fracture. ReWalk Robotics rebranded to Lifeward in 2024. Distinct from the 2017 ReWalk tibia/fibula recall (a recall, not a MAUDE report). Source: FDA MAUDE MDR key 10050473, accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE.
When did this incident occur?
The incident is recorded as occurring on December 18, 2019 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
Who was involved in ReWalk (now Lifeward) Personal 6.0: lateral tibial plateau fracture in a new user (FDA MAUDE)?
The incident is recorded as involving Lifeward on the DEPLOY registry. No specific robot model is linked to this incident in the registry.
Has anyone responded to ReWalk (now Lifeward) Personal 6.0: lateral tibial plateau fracture in a new user (FDA MAUDE)?
No responses to this incident are recorded on the DEPLOY registry. Operators, manufacturers, or affected parties can submit responses to the editorial team; absence is not a guarantee no response was issued.
What is the current status of ReWalk (now Lifeward) Personal 6.0: lateral tibial plateau fracture in a new user (FDA MAUDE)?
This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.
Methodology: Unreviewed · no sources on file · last reviewed 2026-06-27

Verification posture

Unreviewed

Low confidence

Review state

Stable

Last reviewed 2026-06-27

The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.

Methodology surface for ReWalk (now Lifeward) Personal 6.0: lateral tibial plateau fracture in a new user (FDA MAUDE).

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Canonical ID 0682f2d6-4c13-4d6a-86ee-2506a05b824b