QB1 NMES System QB-1000-207Recalls & reported problems
Motive Health, Inc. · QB1 NMES System with Post-Op Brace; S/M, Right · 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 00854691008162), received between Nov 17, 2020 and Nov 17, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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
- Improper or Incorrect Procedure or Method1
- Use of Device Problem1
Patient problems
- Superficial (First Degree) Burn1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 17, 2020Use of Device Problem; Improper or Incorrect Procedure or Method; Use of Device Problem; Improper or Incorrect Procedure or Method
ON OCTOBER 29, 2020 PATIENT CONTACTED CYMEDICA CUSTOMER SERVICE REGARDING BURNS HE RECEIVED FROM THE ELECTRODES. THE "BURN" MARKS ARE HEALED NOW; PLEASE TAKE NOTE THAT HE USED THE SAME SET OF PADS SINCE LATE AUGUST. THE PATIENT DID NOT USE GEL. CUSTOMER SERVICE SHIPPED HIM NEW ELECTRODES AND RE-EDUCATED HIM ON USE/CARE ETC.
Patient problems: Superficial (First Degree) Burn
MAUDE report 10853001 ↗
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- emField 5038Zimmer MedizinSysteme GmbH · Stimulator, Muscle, Powered1 report
- Motive Knee System OT01-1002Motive Health, Inc. · Stimulator, Muscle, Powered1 report
- QB1 NMES System QB-1000-216Motive Health, Inc. · Stimulator, Muscle, 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 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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