MULTI-LINK MINI VISION 1007821-28Recalls & reported problems
Abbott Vascular Inc. · MULTI-LINK MINI VISION Coronary Stent and Stent Delivery System 2.00 mm x 28 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 08717648049422), received between Nov 11, 2016 and Nov 11, 2016 — classified as 1 injury.
The most frequently reported specific device problem is “Detachment Of 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 16, 2026.
Most reported problems
Device problems
- Detachment Of Device Component1
- Failure to Advance1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 11, 2016Detachment Of Device Component; Failure to Advance
IT WAS REPORTED THAT THE 2.0X28 MINI VISION STENT DELIVERY SYSTEM (SDS) REACHED THE PROXIMAL RIGHT CORONARY ARTERY (RCA), BUT WAS UNABLE TO CROSS THE MID RCA. THE DISTAL SHAFT OF THE SDS WITH THE BALLOON AND STENT SEPARATED IN THE ANATOMY. NO ATTEMPT WAS MADE TO PERCUTANEOUSLY REMOVE THE SEPARATED STENT AND BALLOON. THE PATIENT WAS SENT TO SURGERY FOR OPEN HEART BYPASS. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Foreign Body In Patient
MAUDE report 6097765 ↗
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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