Teca TP 902-DMG37-TPRecalls & reported problems
Natus Manufacturing Limited · Disposable Monopolar Green Needle, 37mmx26G (48) per PK · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00382830017626), received between May 25, 2020 and Jun 4, 2020 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Separation” (3 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Material Separation3
Patient problems
- Not Applicable3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 4, 2020Material Separation; Material Separation
MalfunctionMay 28, 2020Material Separation; Material Separation
MalfunctionMay 25, 2020Material Separation; Material Separation
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/S50715-004Technomed Engineering B.V. · Electrode, Needle, Diagnostic Electromyograph1 recall0 reports
- Technomed Europe TE/S50715-001-CTechnomed 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.