All Recalls

95,050 total recalls in our database

Artis zee multi, Model Number 10094139

Siemens Medical Solutions USA

🏥 Medical Devices Class I - Dangerous

A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.

Jun 12, 2019 Other Medical Devices Nationwide View Details →

An update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products.

May 16, 2018 Diagnostic Equipment Nationwide View Details →

AXIOM Artis TA, Model Number 7007755

Siemens Medical Solutions USA

🏥 Medical Devices Class I - Dangerous

A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.

Jun 12, 2019 Other Medical Devices Nationwide View Details →

AXIOM Artis dFC, Model Number 7727717

Siemens Medical Solutions USA

🏥 Medical Devices Class I - Dangerous

A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.

Jun 12, 2019 Other Medical Devices Nationwide View Details →

BrightView SPECT, Model Number 882480

Philips Medical Systems (Cleveland)

🏥 Medical Devices Class I - Dangerous

An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.

Jun 10, 2019 Other Medical Devices Nationwide View Details →

Administration sets assembled with inverted pinch clamp cause the fluid from the distal end of the administration set to be pumped to the proximal end of the tubing when secondary set is used with the primary set. Thus, instead of delivering fluid to the patient, blood may be drawn from the patient if there is space in the drug container to hold extra volume of fluid, under the condition that the reversed pinch clamp is not identified

May 29, 2019 Infusion Pumps View Details →

The monitor displays an error message . The error message states "internal error restart or service".

Jun 5, 2019 Diagnostic Equipment Nationwide View Details →

BrightView X , Model Number 882478

Philips Medical Systems (Cleveland)

🏥 Medical Devices Class I - Dangerous

An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.

Jun 10, 2019 Other Medical Devices Nationwide View Details →

AXIOM Artis BA, Model Number 5904656

Siemens Medical Solutions USA

🏥 Medical Devices Class I - Dangerous

A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.

Jun 12, 2019 Other Medical Devices Nationwide View Details →

RX Daytona, Model Nos. RX4040 and RX4041

Randox Laboratories, Limited

🏥 Medical Devices Class I - Dangerous

There was a report of a malfunction with the sensor which resulted in an increase of temperature leading to melting of internal wires and scorch damage to the internal structure of the instrument.

Jun 24, 2019 Other Medical Devices View Details →