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Lapro-Clip 8886848815Recalls & reported problems

Covidien LP · Absorbable Ligating Clip Cartridge · Class 2 · Implant

All models of Lapro-Clip (8)

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 10884521208469), received between Dec 1, 2021 and Dec 1, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1

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.

  • MalfunctionDec 1, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

    ACCORDING TO THE REPORTER, DURING A LAPAROSCOPIC CHOLECYSTECTOMY PROCEDURE, AFTER THE CLIP WAS UNPACKED, IT WAS FOUND THAT THE ORANGE COMPONENT INSIDE THE CLIP IN THE PACKAGE HAD DETACHED AND COULD NOT BE USED NORMALLY. THE CLIP WAS IMMEDIATELY REPLACED WITH A BRAND-NEW PRODUCT TO COMPLETE THE CASE AND RESOLVE THE ISSUE. THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12910508 ↗

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Sources and updates

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