Skip to content

WECK IPN915087Recalls & reported problems

Teleflex Incorporated · Class 1

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 24026704696448), received between Nov 17, 2021 and Nov 17, 2021 — classified as 1 injury.

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

Patient problems

  • Cardiac Arrest1
  • Hematoma1
  • Hemorrhage/Blood Loss/Bleeding1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryNov 17, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

    7 LIGACLIPS FALLING OFF THE SAPHENOUS VEIN, 2 FROM SIDE BRANCH ON A GRAFTED CORONARY ARTERY, 5 FROM THE LIGHTED END OF THE SAPHENOUS VEIN IN THE DONAU LEG. LIGATION CLIP APPLICATOR IDENTIFIED AND TESTED AND REMOVED FROM CIRCULATION AFTER CONCERNS IDENTIFIED. CLINICAL INCIDENT RAISED AND SERIOUS INVESTIGATION PROCESS COMMENCED AT HOSPITAL. CLINICAL CONSEQUENCES: PEA CARDIAC ARREST WITH EMERGENCY RESTERNOTOMY ON ITU AND ARREST OF BLEEDING FROM BLEEDING SIDE BRANCH OF SAPHENOUS VEIN GRAFT TO CORONARY ARTERY. HAEMATOMA OF DONOR LEG SITE.

    Patient problems: Cardiac Arrest; Hematoma; Hemorrhage/Blood Loss/Bleeding

    MAUDE report 12829616 ↗

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.