iCAST 85407Recalls & reported problems
Atrium Medical Corporation · iCAST COVERED STENT, 8MMX59MMX80CM · 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 00650862854077), received between Aug 23, 2016 and Oct 27, 2017 — classified as 3 injuries.
The most frequently reported specific device problem is “Activation, Positioning or Separation Problem” (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.
Most reported problems
Device problems
- Activation, Positioning or Separation Problem1
- Detachment Of Device Component1
- Leak/Splash1
- Physical Resistance1
Patient problems
- No Code Available2
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 27, 2017Leak/Splash
IT WAS REPORTED THAT ON 3-YEAR FOLLOW UP CT SCAN, A TYPE III ENDOLEAK AT THE OVERLAP OF THE BRANCH GRAFT AND THE STENT WAS NOTED. A TYPE II LUMBAR ENDOLEAK WAS ALSO PRESENT WITHIN THE INFRARENAL ANEURYSM SAC.
Patient problems: No Code Available
MAUDE report 6983669 ↗InjuryOct 10, 2016Activation, Positioning or Separation Problem
InjuryAug 23, 2016Detachment Of Device Component; Physical Resistance
THE PHYSICIAN DEPLOYED THE STENT INTO THE DISTAL AORTA. HE FELT RESISTANCE WHILE TRYING TO PULL THE BALLOON OUT OF THE SHEATH. THE BALLOON BECAME DETACHED INSIDE THE SHEATH. THE PHYSICIAN WAS ABLE TO RETRIEVE THE BALLOON WITH NO COMPLICATIONS.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 5897425 ↗
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.