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Endo Lung 173051Recalls & reported problems

Covidien LP · Clamp · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 10884523000788), received between Dec 5, 2017 and Dec 5, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Open or Close” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Difficult to Open or Close1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionDec 5, 2017Difficult to Open or Close; Difficult to Open or Close

    ACCORDING TO THE REPORTER AN ISSUE OCCURRED DURING PREPARATION FOR A WEDGE / SEGMENTAL RESECTION PROCEDURE. THE JAWS OF THE DEVICE WERE CHECKED AND IT WAS NOTED THAT THEY WOULD NOT OPEN OR CLOSE. THE DEVICE WAS NOT USED ON THE PATIENT. THE PROCEDURE WAS COMPLETED WITH ANOTHER DEVICE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7085819 ↗

Other MOTOR, SURGICAL INSTRUMENT, PNEUMATIC POWERED devices

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Sources and updates

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