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WECK IPN914987Recalls & reported problems

Teleflex Incorporated · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 24026704710205), received between Jun 7, 2022 and Mar 31, 2023 — classified as 2 malfunctions.

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

Most reported problems

Device problems

  • Material Separation1
  • Mechanical Jam1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 31, 2023Material Separation; Material Separation

    REPORTED ISSUE: THE HOLDING PIN ON THE HANDLE FELL FROM THE APPLIER BEFORE USE ON A PATIENT. THE PIN DID NOT FALL/REMAIN IN THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16659814 ↗
  • MalfunctionJun 7, 2022Mechanical Jam; Mechanical Jam

    THE LOADED CLIP GOT STUCK AND DID NOT LEAVE THE APPLIER DURING A SURGERY. THEREFORE, THE USER REPLACED THE APPLIER WITH A NEW UNIT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14619407 ↗

Other Applier, surgical, clip devices

All Applier, surgical, clip devices →

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