Skip to content

TELEFLEX IPN055281Recalls & reported problems

Teleflex Incorporated · Medium Titanium Clips - 1 Cartridge/1 Pouch · Class 2 · Implant

Adverse event reports
3
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 24026704666670), received between Mar 7, 2023 and Mar 7, 2023 — classified as 3 injuries.

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

  • Adverse Event Without Identified Device or Use Problem3

Patient problems

  • Hemorrhage/Blood Loss/Bleeding3
  • Unspecified Tissue Injury3
  • Insufficient Information1

Recent adverse event reports

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

  • InjuryMar 7, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    REPORTED ISSUE: WE HAD AN INCIDENT 10 DAYS AGO WHILE DOING AN AV FISTULA THAT A BLUE LIGATION CLIP WAS APPLIED TO THE VESSEL AND IT SEVERED THE VESSEL CAUSING IT TO RETRACT AND INCREASED THE BLEEDING TO THE ARM.

    Patient problems: Hemorrhage/Blood Loss/Bleeding; Unspecified Tissue Injury

    MAUDE report 16496660 ↗
  • InjuryMar 7, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    REPORTED ISSUE: WE HAD AN INCIDENT 10 DAYS AGO WHILE DOING AN AV FISTULA THAT A BLUE LIGATION CLIP WAS APPLIED TO THE VESSEL AND IT SEVERED THE VESSEL CAUSING IT TO RETRACT AND INCREASED THE BLEEDING TO THE ARM. THIS IS LINKED TO REPORT 3011137372-2023-00026. WE RECEIVED ADDITIONAL CLIPS SAMPLES WITHOUT LOT NUMBERS.

    Patient problems: Hemorrhage/Blood Loss/Bleeding; Unspecified Tissue Injury

    MAUDE report 16496536 ↗
  • InjuryMar 7, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    REPORTED ISSUE: WE HAD AN INCIDENT 10 DAYS AGO WHILE DOING AN AV FISTULA THAT A BLUE LIGATION CLIP WAS APPLIED TO THE VESSEL AND IT SEVERED THE VESSEL CAUSING IT TO RETRACT AND INCREASED THE BLEEDING TO THE ARM.

    Patient problems: Hemorrhage/Blood Loss/Bleeding; Insufficient Information; Unspecified Tissue Injury

    MAUDE report 16496367 ↗

Other CLIP, IMPLANTABLE devices

All CLIP, IMPLANTABLE devices →

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