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Orsiro 3.5/9/140Recalls & reported problems

Biotronik AG · Class 3 · Implant

All models of Orsiro (49)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 07640130438880), received between Apr 4, 2019 and Jun 28, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Failure to Advance” (2 reports).

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

  • Failure to Advance2

Patient problems

  • No Consequences Or Impact To Patient2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 28, 2019Failure to Advance; Failure to Advance

    THE ORSIRO DRUG-ELUTING STENT SYSTEM COULD NOT PASS THE CALCIFIED LESION. NO MORE INFORMATION AVAILABLE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8746041 ↗
  • MalfunctionApr 4, 2019Failure to Advance; Failure to Advance

    IT WAS INTENDED TO CROSS A PREVIOUSLY IMPLANTED STENT WITH AN ORSIRO DRUG-ELUTING STENT SYSTEM TO TREAT A MORE DISTAL LESION. THE PROXIMAL STENT COULD NOT BE CROSSED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8484119 ↗

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Sources and updates

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