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Nitinol Devices and Components Recalls
12 recalls on record · July 2, 2014 to July 2, 2014 · Medical Devices
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Straigh
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire; 0.035 OD, Stiff Shaft, Straight Tip, 180 CM Length; Manufactured for Covidien, P
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Straig
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire;Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire;Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Angled
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Str
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile.Nitinol Guidewire with Hydrophili
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Str
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Ang
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Ang
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.
July 2, 2014Medical DevicesFDA
Nitinol Devices and Components, Inc. recalls HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Ang
Hazard: Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guidewire.