miha bodytec miha bodytec m.oveRecalls & reported problems
miha bodytec GmbH · miha bodytec m.ove is a device which performs electronic muscle stimulation based on EMS technology. The device is specifically designed as an addition to other sports and for training muscles. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04260646650014), received between Dec 19, 2025 and Dec 19, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (2 reports).
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Improper or Incorrect Procedure or Method2
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 19, 2025Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
FIRST-TIME USER EXPERIENCED SEVERED RHABDOMYOLYSIS FOLLOWING AN INITIAL WHOLE-BODY EMS TRAINING SESSION AND WAS HOSPITALIZED FOR APPROXIMATELY FIVE DAYS. THE SESSION WAS CONDUCTED USING A MIHA BODYTEC M.OVE DEVICE IN COMBINATION WITH THE I-BODY CONNECT WIRELESS UNIT AT A CUSTOMER LOCATION. THE USER'S FIRST EMS SESSION LASTED APPROXIMATELY 20 MINUTES OF INTERMITTENT STIMULATION, EXCEEDING THE STANDARD INITIAL SESSION DURATION RECOMMENDED IN THE DEVICE'S INSTRUCTIONS FOR USE.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 23847806 ↗InjuryDec 19, 2025Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
FIRST-TIME USER EXPERIENCED SEVERED RHABDOMYOLYSIS FOLLOWING AN INITIAL WHOLE-BODY EMS TRAINING SESSION AND WAS HOSPITALIZED FOR APPROXIMATELY FIVE DAYS. THE SESSION WAS CONDUCTED USING A MIHA BODYTEC M.OVE DEVICE IN COMBINATION WITH THE I-BODY CONNECT WIRELESS UNIT AT A CUSTOMER LOCATION. THE USER'S FIRST EMS SESSION LASTED APPROXIMATELY 20 MINUTES OF INTERMITTENT STIMULATION, EXCEEDING THE STANDARD INITIAL SESSION DURATION RECOMMENDED IN THE DEVICE'S INSTRUCTIONS FOR USE.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 23847742 ↗
Other Stimulator, Muscle, Powered, For Muscle Conditioning devices
- CoolTone 5034Zimmer MedizinSysteme GmbH · Stimulator, Muscle, Powered, For Muscle Conditioning9 reports
- TENS 7000 Rechargeable DT7303Drive Devilbiss Healthcare · Stimulator, Muscle, Powered, For Muscle Conditioning2 reports
- COMPEX 11-2137Djo, LLC · STIMULATOR, MUSCLE, POWERED, FOR MUSCLE CONDITIONING1 report
- COMPEX 2540660Djo, LLC · STIMULATOR, MUSCLE, POWERED, FOR MUSCLE CONDITIONING1 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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