Lokomat Pro (REF 32001)Recalls & reported problems
Hocoma AG · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 07640174660254), received between May 20, 2022 and May 20, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction 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.
Most reported problems
Device problems
- Patient Device Interaction Problem1
Patient problems
- Impaired Healing1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 20, 2022Patient Device Interaction Problem; Patient Device Interaction Problem
INITIALLY LEFT GLUTEAL FOLD BRUISING AS A RESULT OF LOKOMAT USE. DEVELOPED INTO STAGEABLE IV WOUND.
Patient problems: Impaired Healing
MAUDE report 14462245 ↗
Other Exerciser, Powered devices
- Lokomat Pro 6.3 FD ADHocoma AG · Exerciser, Powered1 report
- Lokomat ProHocoma AG · Exerciser, Powered1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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