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Visu-Loc 2001Recalls & reported problems

Microline Surgical, Inc. · Visu-Loc 5mm Multi-Fire Spring Clip Applier, 20 clips, Disposable · Class 2

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00811099010418), received between Jul 12, 2019 and Jul 12, 2019 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Mechanical Jam” (3 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Mechanical Jam3

Patient problems

  • No Known Impact Or Consequence To Patient3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 12, 2019Mechanical Jam; Mechanical Jam

    CLIP APPLIER JAMMED DURING PROCEDURE. ANESTHESIA TIME WAS EXTENDED 5 MINUTES. THERE WAS NO HARM TO THE PATIENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8784354 ↗
  • MalfunctionJul 12, 2019Mechanical Jam; Mechanical Jam

    CLIP APPLIER JAMMED DURING PROCEDURE. ANESTHESIA TIME WAS EXTENDED 5 MINUTES. THERE WAS NO HARM TO THE PATIENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8784353 ↗
  • MalfunctionJul 12, 2019Mechanical Jam; Mechanical Jam

    CLIP APPLIER JAMMED DURING PROCEDURE. ANESTHESIA TIME WAS EXTENDED 5 MINUTES. THERE WAS NO HARM TO THE PATIENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8784351 ↗

Other Clip, Implantable devices

All Clip, Implantable devices →

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