iCast Covered Stent System, 9mmX38mmX80cm 48938Recalls & reported problems
Atrium Medical Corporation · iCast Covered Stent System, 9mmX38mmX80cm · Class 3 · Implant
Data updated Oct 18, 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 00650862489385), received between Mar 6, 2026 and Jun 10, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Patient-Device Incompatibility” (2 reports).
1 other recall cover devices cleared under the same FDA submission (P120003); they may or may not involve this specific model.
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Patient-Device Incompatibility2
- Inflation Problem1
Patient problems
- Calcium Deposits/Calcification2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 10, 2026Inflation Problem; Patient-Device Incompatibility
IT WAS REPORTED THAT THE BALLOON WOULD NOT INFLATE BEYOND 6 ATM, SO THE BALLOON WAS REMOVED FROM THE ICAST STENT WITHOUT MOVING THE STENT. A NEW 8 MM X 40 MM MUSTANG BALLOON WAS USED ACROSS AND COMPLETED THE EXPANSION OF THE STENT. NO HARM WAS REPORTED.
Patient problems: Calcium Deposits/Calcification
MAUDE report 25457804 ↗MalfunctionMar 6, 2026Patient-Device Incompatibility
THE BALLOON WAS ABLE TO BE INFLATED TO NOMINAL BALLOON INFLATION PRESSURE OF 8 ATM AND THE STENT WAS DEPLOYED.
Patient problems: Calcium Deposits/Calcification
MAUDE report 24530559 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under P120003. One submission often covers many models, so check the product and lot details in each record.
- Z-0291-2024 · Sep 21, 2023 · Open, ClassifiedAtrium Advanta V12 Covered Stent System, 10mm x 59mm x 80cm (OUS)-Indicated for restoring and improving the patency of the iliac andrenal arteries. Renal approval includes 5mm, 6m
Other Iliac Covered Stent, Arterial devices
- GORE VIABAHN VBX Balloon Expandable Endo BXB073902AW. L. Gore & Associates, Inc. · Iliac covered stent, arterial1 recall2 deaths19 reports
- iCast Covered Stent System, 6mmX16mmX120cm 42616Atrium Medical Corporation · Iliac Covered Stent, Arterial1 recall15 reports
- GORE VIABAHN VBX Balloon Expandable Endo BXB057902AW. L. Gore & Associates, Inc. · Iliac covered stent, arterial1 recall2 deaths14 reports
- GORE VIABAHN VBX Balloon Expandable Endo BXB067902AW. L. Gore & Associates, Inc. · Iliac covered stent, arterial1 recall14 reports
- GORE VIABAHN VBX Balloon Expandable Endo BXB075902AW. L. Gore & Associates, Inc. · Iliac covered stent, arterial1 recall11 reports
- GORE VIABAHN VBX Balloon Expandable Endo BXB095902AW. L. Gore & Associates, Inc. · Iliac covered stent, arterial1 recall8 reports
- GORE VIABAHN VBX Balloon Expandable Endo BXB077902AW. L. Gore & Associates, Inc. · Iliac covered stent, arterial1 recall8 reports
- GORE VIABAHN VBX Balloon Expandable Endo BXB085902AW. L. Gore & Associates, Inc. · Iliac covered stent, arterial1 recall2 deaths8 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page