PILLING IPN915273Recalls & reported problems
Teleflex Incorporated · PUNCH DP-52K DISPOSABLE PUNCH 5.2 MILLIMETERS · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 14026704697974), received between Apr 9, 2024 and Nov 13, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Mechanical Jam” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Mechanical Jam2
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Perforation of Vessels1
- Vascular Dissection1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryNov 13, 2024Mechanical Jam; Mechanical Jam
IT WAS REPORTED THAT "DURING A KIDNEY TRANSPLANT, WHEN PREPARING THE ARTERIAL ANASTOMOSIS, THE PUNCH BECAME STUCK JAMMED IN THE ARTERY. TEAR OF THE ARTERIAL WALL". AT THE TIME OF THIS REPORT, THE CUSTOMER HAS NOT RETURNED OUR REQUESTS FOR ADDITIONAL INFORMATION.
Patient problems: Vascular Dissection
MAUDE report 20678074 ↗InjuryApr 9, 2024Mechanical Jam; Mechanical Jam
IT WAS REPORTED THAT "DURING USE, PUNCH GETS JAMMED IN THE ARTERIA". ADDITIONAL INFORMATION RECEIVED STATES THAT "THE PUNCH TORE THE ARTERY AT THE TIME OF RELEASING AND PERFORATED THE ARTERY. THE ARTERY HAD TO BE CUT TO REMOVE THE PUNCH. ARTERIAL REPAIR WAS REQUIRED TO PREVENT BLEEDING. THE PATIENT IS FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions; Perforation of Vessels
MAUDE report 19071944 ↗
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- ADVANTA SLIDER GDS 22092Atrium Medical Corporation · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- PILLING IPN005932Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR18 reports
- PILLING IPN915270Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR16 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.