Skip to content

PILLING IPN917591Recalls & reported problems

Teleflex Incorporated · PUNCH MDP-60K DISPOSABLE PUNCH 6.0 MILLIMETERS · Class 1

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704735508), received between Nov 7, 2022 and Nov 7, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (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

  • Physical Resistance/Sticking1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • MalfunctionNov 7, 2022Physical Resistance/Sticking; Physical Resistance/Sticking

    IT WAS REPORTED THAT THE CUSTOMER HAS HAD MULTIPLE CASES WHERE THE PUNCHES HAVE BEEN STICKING. THE PATIENT'S CONDITION IS UNKNOWN.

    Patient problems: Insufficient Information

    MAUDE report 15749071 ↗

Other INSTRUMENTS, SURGICAL, CARDIOVASCULAR devices

All INSTRUMENTS, SURGICAL, CARDIOVASCULAR devices →

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