iCAST 85409Recalls & reported problems
Atrium Medical Corporation · iCAST COVERED STENT, 9MMX59MMX80CM · Class 2 · Implant
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00650862854091), received between Sep 26, 2017 and Oct 16, 2023 — classified as 3 injuries.
The most frequently reported specific device problem is “Device Operates Differently Than Expected” (1 report).
2 other recalls cover devices cleared under the same FDA submission (K050814); 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Device Operates Differently Than Expected1
- Premature Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Code Available1
- Occlusion1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 16, 2023Premature Separation; Premature Separation
WHILE THE VASCULAR SURGEON WAS DEPLOYING AN ICAST STENT IN ILIAC ARTERY, DEPLOYED THROUGH 7F SHEATH. EVERYTHING WENT AS NORMAL, STENT DEPLOYED IN ILIAC ARTERY AND NOTICED BALLOON DETACHED FROM DELIVERY SYSTEM DURING REMOVAL OF DELIVERY CATHETER. BALLOON WAS SNARED AND REMOVED THROUGH SHEATH. NO ADVERSE ISSUES TO PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17941134 ↗InjurySep 20, 2018Appropriate Device Problem Term/Code Not Available
InjurySep 26, 2017Device Operates Differently Than Expected
IT WAS REPORTED THAT THE STENT DID NOT CROSS A 100% LEFT COMMON ILIAC ARTERY OCCLUSION. THE STENT WAS NOT DEPLOYED.
Patient problems: Occlusion
MAUDE report 6894783 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K050814. One submission often covers many models, so check the product and lot details in each record.
- Z-1077-2022 · Mar 3, 2022 · Open, ClassifiediCast Covered Stent System Product Code/Part Number: 85400 85401 85402 85403 85404 85405 85406 85407 85408 85409 85410 85411 85412 85413 85414 85415 85416 8541
- Z-2761-2017 · May 25, 2017 · TerminatedAtrium iCAST Balloon Expandable Covered Stent; 7mm x 22mm x 120cm; Model/Part Number 85455 (Marketed in U.S. only) Atrium Advanta V12 Balloon Expandable Covered Stent; 7mm x 22mm
Other Prosthesis, tracheal, expandable devices
- iCAST 85453Atrium Medical Corporation · Prosthesis, tracheal, expandable43 reports
- WALLSTENT™ BILIARY H965430500Boston Scientific Corporation · Prosthesis, tracheal, expandable13 reports
- iCAST 85419Atrium Medical Corporation · Prosthesis, tracheal, expandable13 reports
- iCAST 85445Atrium Medical Corporation · Prosthesis, tracheal, expandable12 reports
- iCAST 85416Atrium Medical Corporation · Prosthesis, tracheal, expandable12 reports
- iCAST 85455Atrium Medical Corporation · Prosthesis, tracheal, expandable11 reports
- WALLSTENT® Endoprosthesis H965404130Boston Scientific Corporation · Prosthesis, tracheal, expandable11 reports
- iCAST 85414Atrium Medical Corporation · Prosthesis, tracheal, expandable10 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.