MULTI-LINK MINI VISION 1007822-08Recalls & reported problems
Abbott Vascular Inc. · MULTI-LINK MINI VISION Coronary Stent and Stent Delivery System 2.25 mm x 08 mm / Rapid-Exchange · Class 3 · Implant
All models of MULTI-LINK MINI VISION (16)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08717648049439), received between Sep 4, 2018 and Sep 4, 2018 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Angina1
- Dizziness1
- Myocardial Infarction1
- Occlusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 4, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED BY THE PATIENT THAT HE HAD A MYOCARDIAL INFARCTION IN THE RIGHT CORONARY ARTERY (RCA) ON (B)(6) 2013. FOUR VISION STENTS WERE IMPLANTED EMERGENTLY AT (B)(6) BY DR. (B)(6). A MINI VISION RX 2.25 X 8 MM AND A VISION RX 2.75 X 15 MM WERE IMPLANTED IN THE MID RCA, A MINI VISION RX 2.5 X 15 MM WAS IMPLANTED IN THE PROXIMAL RCA, AND A MINI VISION RX 2.5 X 12 MM WAS IMPLANTED IN THE DISTAL RCA. FOUR YEARS LATER, THE PATIENT WAS RE-ADMITTED ON (B)(6) 2017 WITH LIGHTHEADEDNESS, DIZZINESS, ANGINA AND ANOTHER MYOCARDIAL INFARCTION. THE PATIENT STATED HE WAS TOLD THAT ALL FOUR OF THE PREVIOUSLY PLACED STENTS WERE 100% BLOCKED; ALTHOUGH HE WAS NOT TOLD WHETHER THIS WAS DUE TO THROMBOSIS OR RE-STENOSIS. TWO ADDITIONAL UNKNOWN STENTS WERE EMERGENTLY IMPLANTED AS TREATMENT AT (B)(6) BY DR. (B)(6). NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Angina; Dizziness; Myocardial Infarction; Occlusion
MAUDE report 7843580 ↗
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- 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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