Products: rehab-exoskeleton. Risk band: Low RobotRisk index 7.0/100 (incidents/exposure, time-weighted) · 88th percentile of 162 medical robotics companies.
Motek Medical's record consists of a single FDA Class II recall, dated July 2019, for the Body Weight Support (BWS) Light component of the C-Mi rehabilitation system, severity 3. This is a regulatory-driven record originating from an FDA recall action rather than a field-incident press report. The single entry shows no trajectory or repeat pattern. The index of 7.1 places Motek Medical at the 88.2 percentile within medical-robotics, indicating a low risk standing among category peers.
| Sev | Date | Type | Location | Incident | Source |
|---|---|---|---|---|---|
| S3 | 07/29 2019 |
recall | — | FDA Class II recall: Body Weight Support (BWS) Light; Model No. RB011; a component of C-Mil · Body Weight Support (BWS) Light; Model… | openFDA enforcement |