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FDA Class 1 Recall on iCast Stent for Separation Risk That May Cause Harm

Published: June 6, 2022

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death

Source: dicardiology.com

Related Topics:

United StatesAtrium Medical CorporationAdverse Event Reporting ProgramDrug AdministrationCast Covered Stent SystemCast CoveredLot NumbersCast Covered StentAtrium MedicalUrgent Medical Device CorrectionWatch Safety Information

Atrium Recalls iCast Stent for Separation Risk That May Cause Harm

Published: June 2, 2022

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death

Source: dicardiology.com

Related Topics:

United StatesAtrium Medical CorporationAdverse Event Reporting ProgramCast Covered Stent SystemCast CoveredLot NumbersMedical CorporationCast Covered StentAtrium MedicalUrgent Medical Device CorrectionWatch Safety Information