PILLING IPN917586Recalls & reported problems
Teleflex Incorporated · PUNCH MDP-40K DISPOSABLE PUNCH 4.0 MILLIMETERS · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 14026704735454), received between Nov 7, 2022 and Nov 7, 2022 — classified as 1 injury, 1 malfunction.
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.
Most reported problems
Device problems
- Mechanical Jam2
Patient problems
- Insufficient Information1
- Unspecified Tissue Injury1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryNov 7, 2022Mechanical Jam; Mechanical Jam
IT WAS REPORTED THAT THEY JUST DID A KIDNEY/PANCREAS TRANSPLANT AND THE PUNCH GO STUCK AND IT HAD TO BE CUT OUT. THE PATIENT'S CONDITION IS UNKNOWN.
Patient problems: Unspecified Tissue Injury
MAUDE report 15749506 ↗MalfunctionNov 7, 2022Mechanical Jam; Mechanical Jam
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 15749084 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.