PILLING IPN056405Recalls & reported problems
Teleflex Incorporated · PUNCH MDP-40K DISPOSABLE PUNCH 4.0 MILLIMETERS · Class 1
All models of PILLING (28)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 14026704714169), received between May 4, 2021 and May 4, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Misfire” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Misfire2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 4, 2021Misfire; Misfire
WE HAD TWO MISFIRE IN A CASE LAST WEEK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11769609 ↗MalfunctionMay 4, 2021Misfire; Misfire
WE HAD TWO MISFIRE IN A CASE LAST WEEK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11769589 ↗
Other INSTRUMENTS, SURGICAL, CARDIOVASCULAR devices
- ACCESSRAIL Platform (Standard Blade) SB-1000Maquet Cardiovascular LLC · Instruments, Surgical, Cardiovascular1 recall6 reports
- ADVANTA SLIDER GDS 22025Atrium Medical Corporation · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- ADVANTA SLIDER GDS 22092Atrium Medical Corporation · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- Needle NDL-107-04Galt Medical Corp. · Instruments, Surgical, Cardiovascular1 recall0 reports
- ADVANTA SLIDER GDS 22125Atrium Medical Corporation · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- Lead Clippers G20003Cook Vandergrift Inc. · 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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