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Lapro-Clip 8886848799Recalls & reported problems

Covidien LP · Reusable Clip Remover · Class 1

All models of Lapro-Clip (8)

Data updated Oct 16, 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 10884521057616), received between Jan 7, 2020 and Feb 14, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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 16, 2026.

Most reported problems

Device problems

  • Break1
  • Difficult to Open or Close1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Patient Involvement1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 14, 2022Difficult to Open or Close; Difficult to Open or Close

    ACCORDING TO THE REPORTER, PRIOR TO USE, EVEN THOUGH THE GRIP WAS SQUEEZED, THE JAWS PART, WHICH FOR CLAMPING THE TIP AND THE CLIP, WERE IN THE STATE THAT COULD NOT BE OPENED AND CLOSED. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13528053 ↗
  • MalfunctionJan 7, 2020Break; Break

    ACCORDING TO THE REPORTER, DURING THE DEMONSTRATION, THE TIP OF THE HOOK WAS FOUND TO BE CHIPPED. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Patient Involvement

    MAUDE report 9561921 ↗

Sources and updates

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