Johari Digital Healthcare Limited NeubieRecalls & reported problems
Syrma Johari Medtech Limited · Electronic muscle stimulator · Class 2
Data updated Oct 18, 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 08908008085253), received between May 7, 2022 and May 7, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Muscle Weakness/Atrophy1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 7, 2022Insufficient Device Problem Information; Insufficient Device Problem Information
(B)(6) WAS A CLIENT OF EVO PERFORMANCE. ON (B)(6) 2021, (B)(6) HAD A TRAINING SESSION. LATER SHE WAS DIAGNOSED WITH RHABDOMYOLYSIS. THIS WAS UNKNOWN TO NEUFIT UNIT SHE POSTED HER NEGATIVE EXPERIENCE ON NEUFIT'S (B)(6) ON (B)(6) 2022. NEUFIT REACHED OUT TO EVO PERFORMANCE FOR MORE INFORMATION AND WAS PROVIDED AN DESCRIPTION OF HER WORKOUT ALONG WITH THE WAIVERS SHE SIGNED. (B)(6) REACHED OUT TO (B)(6) FOR MORE INFORMATION AND SHE DID NOT REPLY.
Patient problems: Muscle Weakness/Atrophy
MAUDE report 14331964 ↗
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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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