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Teca Elite 902-DMF25-SRecalls & reported problems

Natus Manufacturing Limited · TECA Elite Disposable Monopolar Red Needle, 25mmx28G (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 00382830017534), received between Jan 23, 2021 and Feb 26, 2021 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Separation Failure” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Separation Failure2

Patient problems

  • No Clinical Signs, Symptoms or Conditions3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 26, 2021Separation Failure; Separation Failure

    NEEDLES PULLED AWAY FROM THE HUB. NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11387044 ↗
  • MalfunctionFeb 18, 2021Separation Failure; Separation Failure

    HUB IS PULLING OFF THE NEEDLE WHEN REMOVING FROM PATIENT. NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11345651 ↗
  • MalfunctionJan 23, 2021

    HUB IS PULLING OFF THE NEEDLE WHEN REMOVING FROM PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11220385 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.