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Other Medical Devices

🏥 Medical Devices 15,809 recalls

Software defect. In certain circumstances, the application may display incorrect measurements of cardiac and aortic anatomy used to select and size the Transcatheter heart valve (THV) to be implanted .

Nov 9, 2014 Other Medical Devices View Details →

Non-sterile drape

Novadaq Technologies

Class I - Dangerous

Non sterile-drape LUNA drape was inadvertently mislabeled with an additional contents sterile label.

Nov 4, 2014 Other Medical Devices Nationwide View Details →
Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details →
Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details →
Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details →

Software upgrade to correct potential safety issue related to CyberKnife System that occurs when upgrading the Treatment Delivery Software for the first generation Iris Variable Aperture Collimator.

Oct 31, 2014 Other Medical Devices Nationwide View Details →
Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details →

When the MC-500 is turned on and coagulation is performed without changing the laser color, the delivery unit occasionally fails to emit the laser, or the power output is lower than the set program.

Oct 24, 2012 Other Medical Devices View Details →
Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details →
Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details →

SPHERES 8801071 1/TRAY 12PK

Medtronic Navigation

Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details →
Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details →
Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details →

SPHERES 8801075 5/TRAY 12PK

Medtronic Navigation

Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details →

The 10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM (Sterile) was assembled incorrectly. If the non conformance goes undetected, it may impact the locking function post-operatively and compromise the bone reduction and construct stability which may lead to non-union/malunion.

Oct 29, 2014 Other Medical Devices View Details →