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ReWalk(TM) Personal 6.0
LIFEWARD LTD · Model 50-20-0004 · UDI-DI 00861803000303
PHL
Prescription
1
510(k) clearances
57
Adverse events
3
Recalls
8
Facilities
Description
Powered Exoskeleton - community use
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-04-03 | WANDERCRAFT SAS | Potential for exoskeleton to lose lateral balance and cause patient to fall. |
| 2020-02-28 | Argo Medical Technologies Ltd | ReWalk Robotics received two complaints (one in the US; one in the Germany), which alleged that the ReWalk device waistpack (which is the location of the Li-Ion battery packs) caug |
| 2017-08-14 | Argo Medical Technologies Ltd | Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.