Class IIOngoingZ-2464-2026
ConMed Corporation recalls ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip
Potential for overpressure alerts.
ConMed CorporationNYJun 24, 2026
Recalls in New York
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 13–24 of 82 recalls
Class IIOngoingZ-1875-2026
Angiodynamics, Inc. recalls AccuVu Angiographic Catheter
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics, Inc.NYApr 29, 2026
Class IIOngoingZ-1874-2026
Angiodynamics, Inc. recalls AccuVu Angiographic Catheter
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics, Inc.NYApr 29, 2026
Class IIOngoingZ-1873-2026
Angiodynamics, Inc. recalls AccuVu Angiographic Catheter
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics, Inc.NYApr 29, 2026
Class IIOngoingZ-1872-2026
Angiodynamics, Inc. recalls AccuVu Angiographic Catheter
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics, Inc.NYApr 29, 2026
Class IIOngoingZ-1871-2026
Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics, Inc.NYApr 29, 2026
Class IIOngoingZ-1870-2026
Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics, Inc.NYApr 29, 2026
Class IIOngoingZ-1869-2026
Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics, Inc.NYApr 29, 2026
Class IIOngoingZ-1868-2026
Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics, Inc.NYApr 29, 2026
Class IIOngoingZ-1867-2026
Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics, Inc.NYApr 29, 2026
Class IIOngoingZ-1866-2026
Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics, Inc.NYApr 29, 2026
Class IIOngoingZ-1865-2026
Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics, Inc.NYApr 29, 2026