PILLING IPN915269Recalls & reported problems
Teleflex Incorporated · PUNCH DP-36K DISPOSABLE PUNCH 3.6 MILLIMETERS · Class 1
All models of PILLING (28)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 14026704697936), received between Apr 2, 2024 and Apr 2, 2024 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (4 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Cut4
Patient problems
- Insufficient Information4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 2, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT DURING A RENAL TRANSPLANT CASE PERFORMING AN ARTERIAL ANASTOMOSIS, "THE PUNCH GOT JAMMED. SCISSORS WERE USED TO CUT AROUND THE PUNCH TO REMOVE THE DEVICE". NO REPORT OF PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS "UNKNOWN".
Patient problems: Insufficient Information
MAUDE report 19028752 ↗MalfunctionApr 2, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT DURING A RENAL TRANSPLANT CASE PERFORMING AN ARTERIAL ANASTOMOSIS, "THE PUNCH GOT JAMMED. SCISSORS WERE USED TO CUT AROUND THE PUNCH TO REMOVE THE DEVICE". NO REPORT OF PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS "UNKNOWN".
Patient problems: Insufficient Information
MAUDE report 19028280 ↗MalfunctionApr 2, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT DURING A RENAL TRANSPLANT CASE PERFORMING AN ARTERIAL ANASTOMOSIS, "THE PUNCH GOT JAMMED. SCISSORS WERE USED TO CUT AROUND THE PUNCH TO REMOVE THE DEVICE". NO REPORT OF PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS "UNKNOWN".
Patient problems: Insufficient Information
MAUDE report 19027975 ↗MalfunctionApr 2, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT DURING A RENAL TRANSPLANT CASE PERFORMING AN ARTERIAL ANASTOMOSIS, "THE PUNCH GOT JAMMED. SCISSORS WERE USED TO CUT AROUND THE PUNCH TO REMOVE THE DEVICE. THE VESSELS WERE NOT CALCIFIED AND THE SURGEON DOES NOT CLASSIFY THEM AS CHALLENGING CASES". NO REPORT OF PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS "THE PATIENT IS LEFT WITH A DENSELY FIBROUS ANASTOMOTIC STRICTURE WHICH IS DIFFICULT TO MANAGE".
Patient problems: Insufficient Information
MAUDE report 19027725 ↗
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- ADVANTA SLIDER GDS 22125Atrium Medical Corporation · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- PILLING IPN005932Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR18 reports
- PILLING IPN915270Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR16 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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