Lokomat Pro (REF 30682)Recalls & reported problems
Hocoma AG · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07640174660155), received between May 28, 2026 and May 28, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Use of Device Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- Bone Fracture(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 28, 2026Use of Device Problem
PATIENT LOOSES SHOE AND DRAGS TOES ON TREADMILL OF ROBOTIC REHABILITATION DEVICE. LOKOMAT WAS STOPPED BY THERAPIST AND TRAINING CONTINUED. X-RAY ON (B)(6) 26. REVEALED DISTAL FRACTURES OF TIBIA AND FIBULA.
Patient problems: Bone Fracture(s)
MAUDE report 25318307 ↗
Other Exerciser, Powered devices
- Lokomat Pro 6.3 FD ADHocoma AG · Exerciser, Powered1 report
- Lokomat ProHocoma AG · Exerciser, Powered1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.