Oscar 4.0/20-180/80Recalls & reported problems
Biotronik AG · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07640130455740), received between Oct 19, 2022 and Oct 19, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Puncture/Hole” (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
- Material Puncture/Hole1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 19, 2022Material Puncture/Hole; Material Puncture/Hole
AN OSCAR PERIPHERAL MULTIFUNCTIONAL CATHETER SYSTEM WAS SELECTED FOR TREATMENT. THE BALLOON HAD A PINHOLE RUPTURE IN HIGHLY CALCIFIED LESION. THE BALLOON COULD HAVE BEEN DEFLATED AND RETRIEVED FROM THE OSCAR SUPPORT CATHETER, NO OSCAR RELATED COMPLICATION OCCURRED. PHYSICIAN COMMENTED THAT ANY BALLOON WOULD RUPTURE IN A CALCIUM CHUNK LIKE THAT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15632883 ↗
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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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