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WECK IPN914959Recalls & reported problems

Teleflex Incorporated · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 24026704710052), received between Feb 28, 2023 and May 11, 2023 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1
  • Unsealed Device Packaging1

Patient problems

  • Hemorrhage/Blood Loss/Bleeding1
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionMay 11, 2023Unsealed Device Packaging; Unsealed Device Packaging

    IT WAS REPORTED UPON INCOMING INSPECTION, THE PACKAGING SEAL WAS FOUND OPEN. NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16915912 ↗
  • InjuryFeb 28, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

    REPORTED ISSUE: REPORTED ISSUE: MULTIPLE CARDIAC POST-OP BLEEDS AS A RESULT OF LIGATING CLIPS COMING OFF ARTERIAL BRANCHES. THE PATIENT'S CONDITION IS UNKNOWN.

    Patient problems: Hemorrhage/Blood Loss/Bleeding

    MAUDE report 16453305 ↗

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.