MULTI-LINK VISION 1007847-23Recalls & reported problems
Abbott Vascular Inc. · MULTI-LINK RX VISION Coronary Stent System 2.75 mm x 23 mm · Class 3 · Implant
All models of MULTI-LINK VISION (19)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08717648050589), received between Jul 24, 2017 and Jul 24, 2017 — classified as 1 death.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Device Dislodged or Dislocated1
- Failure to Advance1
Patient problems
- Death1
- Vessel Or Plaque, Device Embedded In1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
DeathJul 24, 2017Failure to Advance; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PRESENTED WITH SHORTNESS OF BREATH AND CHEST/SHOULDER PAIN, AND ST ELEVATION MYOCARDIAL INFARCTION WAS DIAGNOSED. CARDIOPULMONARY RESUSCITATION (CPR) WAS INITIATED. THE PATIENT WAS TRANSFERRED TO THE CARDIAC CATHETERIZATION LAB AND UNDERWENT A CORONARY PROCEDURE TO TREAT A TARGET LESION IN THE RIGHT CORONARY ARTERY (RCA). THE 2.75 X 23 MM VISION STENT DELIVERY SYSTEM WAS ADVANCED TO THE TARGET LESION IN THE RIGHT CORONARY ARTERY (RCA); HOWEVER, THE STENT DELIVERY SYSTEM WAS UNABLE TO CROSS DUE TO THE PATIENT ANATOMY AND WAS REMOVED. UPON REMOVAL, IT WAS NOTED THAT THE STENT WAS NOT ON THE DELIVERY SYSTEM. ON ANGIOGRAPHY, THE STENT WAS SEEN AT THE OSTIUM OF THE RCA. A BALLOON DILATATION CATHETER WAS ADVANCED TO THE SITE AND CRUSHED THE STENT TO THE VESSEL WALL, AT THE OSTIUM OF THE RCA. THE 2.75 X 15 MM VISION STENT DELIVERY SYSTEM WAS THEN ADVANCED; HOWEVER, THIS STENT DELIVERY SYSTEM WAS ALSO UNABLE TO CROSS, DUE TO THE PATIENT ANATOMY AND POSSIBLY DUE TO 2.75 X 23 MM VISION STENT CRUSHED TO THE VESSEL WALL, AND WAS REMOVED. THROUGHOUT THE PROCEDURE, CPR CONTINUED. THE GUIDE WIRE AND GUIDE CATHETER LOST VESSEL ACCESS, POSSIBLY DUE TO THE CONTINUED CPR AND
Patient problems: Death; Vessel Or Plaque, Device Embedded In
MAUDE report 6736592 ↗
Other STENT, CORONARY devices
- WALLSTENT® Endoprosthesis H965403130Boston Scientific Corporation · STENT, CORONARY35 reports
- WALLSTENT® Endoprosthesis H965402130Boston Scientific Corporation · STENT, CORONARY23 reports
- Tryton Side Branch Stent T5-2530-191-USTryton Medical, Inc. · Stent, Coronary1 death22 reports
- WALLSTENT® Endoprosthesis H965403330Boston Scientific Corporation · STENT, CORONARY21 reports
- WALLSTENT® Endoprosthesis H965403320Boston Scientific Corporation · STENT, CORONARY10 reports
- WALLSTENT® Endoprosthesis H965403120Boston Scientific Corporation · STENT, CORONARY9 reports
- PALMAZ Balloon Expandable Stent P308Cordis US Corp. · STENT, CORONARY7 reports
- Cobra PzF 170-03-35024Celonova Biosciences, Inc. · Stent, Coronary7 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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