🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
All Recalls
95,018 total recalls in our database
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
BV Endura with Software Release 2.3- A mobile, diagnostic X-ray image acquisition and viewing system. Model Number: 718075
Philips North America
🏥 Medical Devices Class I - Dangerous
Instructions for Use do not specify the maximum surface temperature of the X-ray tank (assembly housing the X-ray tube, beam filter & cooling oil) and the image intensifier/detector of the system as required an result in burns
🏥 Medical Devices Class I - Dangerous
Intermittent risk of electric shock to users if an affected charger is used in conjunction with a faulty or bypassed institutions Mains Protective Earth (Ground) circuit
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
Veradius Unity with Software Release 2.1- Amobile, diagnostic X-ray imaging and viewing system. . Model Number: 718132
Philips North America
🏥 Medical Devices Class I - Dangerous
Instructions for Use do not specify the maximum surface temperature of the X-ray tank (assembly housing the X-ray tube, beam filter & cooling oil) and the image intensifier/detector of the system as required an result in burns
🏥 Medical Devices Class I - Dangerous
The languages for Russian, Romanian, Slovak, and Czech have the power settings for high and low switched in the device.
BV Pulsera with Software Release 2.3-A mobile, diagnostic X-ray image acquisition and viewing system. Model Number: 718095
Philips North America
🏥 Medical Devices Class I - Dangerous
Instructions for Use do not specify the maximum surface temperature of the X-ray tank (assembly housing the X-ray tube, beam filter & cooling oil) and the image intensifier/detector of the system as required an result in burns
O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing Instructions (model preparation for tooth movement) MKT-LB-002 Rev 1 for Orchestrate3d Software v.3.1 - v5.0.4
Orchestrate Orthodontic Technologies
🏥 Medical Devices Class I - Dangerous
Due to product label/labeling being altered from it's approved state.
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
Due to consoles not in compliance with the latest electrical safety standards IEC 60601 and as a result shocked a patient.
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.
🏥 Medical Devices Class I - Dangerous
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.