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WECK IPN915190Recalls & 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 24026704697834), received between Jun 29, 2022 and Mar 10, 2023 — classified as 2 malfunctions.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Improper or Incorrect Procedure or Method1
  • Material Twisted/Bent1

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 10, 2023Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

    REPORTED ISSUE: CLIPS BROKE WHEN THEY WERE TRYING TO LOAD THEM. NO REPORTED INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16525030 ↗
  • MalfunctionJun 29, 2022Material Twisted/Bent; Material Twisted/Bent

    THE TIP OF THE APPLIER WAS BENT IT WAS USED IN UPPER GI CASE. THEY NOTICED THE TIP BENT AT THE END OF THE PROCEDURE. THE PATIENT WAS FINE THE APPLIER WORKED FINE THROUGH THE PROCEDURE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14852861 ↗

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.