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PILLING IPN005737Recalls & reported problems

Teleflex Incorporated · Class 2

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 24026704520279), received between Nov 17, 2021 and Nov 17, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Activation, Positioning or Separation Problem” (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

  • Activation, Positioning or Separation Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionNov 17, 2021Activation, Positioning or Separation Problem; Activation, Positioning or Separation Problem

    IT IS BEING REPORTED BY A SURGEON AS NOT CLAMPING PROPERLY. WHEN USED DURING AN ABDOMINAL AORTIC ANEURYSM IT DID NOT COMPLETELY OCCLUDE BLOOD FLOW. ANOTHER CLAMP WAS USED. NO PATIENT INJURY REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12829471 ↗

Other CLAMP, VASCULAR devices

All CLAMP, VASCULAR devices →

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