Integrity INT27522UXRecalls & reported problems
Medtronic, Inc. · Stent INT27522UX INTEGRITY 2.75X22UX · Class 3 · Implant
All models of Integrity (27)
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 00613994798862), received between Jun 13, 2018 and Jun 13, 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
- Reaction1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 13, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT BEGAN TO GET RASHES APPROXIMATELY 3 MONTHS POST IMPLANT OF AN INTEGRITY BARE METAL STENT. SYMPTOMS INCLUDE ITCHY RED RASH ON ARMS, ABDOMEN, AND BACK, FOR WEEKS TO MONTHS. THE PATIENT CONSULTED A DERMATOLOGIST TO NO AVAIL, AND IS NOW SEEKING CONSULTATION OF AN ALLERGIST. A HEALTH CARE PROFESSIONAL CALLED TO INQUIRE ABOUT THE CONTENT OF THE METAL STENT. THEY WERE INFORMED THAT THERE ARE VARIOUS METALS COMBINED WITHIN THE STENT.
Patient problems: Reaction
MAUDE report 7596367 ↗
Other STENT, CORONARY devices
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- 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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