Myoject MJT-3726-LLRecalls & reported problems
Natus Manufacturing Limited · Disposable Injectable MyoJect Orange Luer Lock NEEDLE 37mm x 0.41mm, 10 per Pk · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382830017725), received between Mar 30, 2021 and Mar 30, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
- Detachment of Device or Device Component1
- Entrapment of Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 30, 2021Break; Entrapment of Device; Detachment of Device or Device Component; Break
BOTOX WAS BEING ADMINISTERED BY PHYSICIAN WITH EMG GUIDANCE INTO RIGHT MID-CALF.UPON REMOVAL OF INJECTION NEEDLE, PHYSICIAN NOTED THERE WAS NOT A NEEDLE ATTACHED AND IT WAS IN THE PATIENT'S BODY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11588368 ↗
Other Electrode, Needle, Diagnostic Electromyograph devices
- Technomed Europe TE/S50715-001Technomed Engineering B.V. · Electrode, Needle, Diagnostic Electromyograph1 recall2 reports
- Technomed Europe TE/S46-638Technomed Engineering B.V. · Electrode, Needle, Diagnostic Electromyograph1 recall2 reports
- Technomed Europe TE/S50715-001-CTechnomed Engineering B.V. · Electrode, Needle, Diagnostic Electromyograph1 recall0 reports
- Technomed Europe TE/S50715-004Technomed Engineering B.V. · Electrode, Needle, Diagnostic Electromyograph1 recall0 reports
- N/A 8227410Medtronic Xomed, Inc. · Electrode, needle, diagnostic electromyograph12 reports
- Teca Elite S53153Natus Manufacturing Limited · Electrode, Needle, Diagnostic Electromyograph7 reports
- Dantec 9013S0032Natus Manufacturing Limited · Electrode, Needle, Diagnostic Electromyograph6 reports
- Dantec 9013S0042Natus Manufacturing Limited · Electrode, Needle, Diagnostic Electromyograph4 reports
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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