Medline MDS6PML1Recalls & reported problems
Medline Industries, Inc. · ANGIOLOCK,MED/LRG,POLY,6/CT,14CT/BX · Class 2 · Implant
- 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 20193489144779), received between Mar 25, 2026 and Mar 30, 2026 — classified as 2 malfunctions.
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.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available2
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 30, 2026Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE FACILITY, ON (B)(6) 2026, "DURING A ROBOT CHOLECYSTECTOMY WITH CHOLANGIOGRAM PROCEDURE, MEDIUM/LARGE CLIPS WOULDN'T LOCK/STAY CLOSED WHEN SURGEON WAS TRYING TO CLIP THE ARTERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24719886 ↗MalfunctionMar 25, 2026Appropriate Device Problem Term/Code Not Available
USE OF ANGIOLOCK MEDIUM/LARGE LIGATION CLIPS DURING PROCEDURE FAILED TO ENGAGE NUMEROUS TIMES. TRIED ANOTHER PACK AND SAME THING OCCURRED. HAD TO USE A DIFFERENT KIND OF CLIPS TO SUCCESSFULLY COMPLETE PROCEDURE.
Patient problems: Insufficient Information
MAUDE report 24688110 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.