Complete FDA and NHTSA recall records dated in March 2025.
These records include useful source details for the selected month.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
Their is a potential of fluid leakage from the centrifugal blood pump pump during the priming procedure or during clinical procedures.
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
Due to an increase in complaints concerning foot tray pedal spring failing resulting in the pedal remaining pressed
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Affected devices have a smaller diameter than expected and may potentially result in inadequate ventilation to the patient. Patient may experience hypoxia, underdose, or cardiopulmonary…
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Retroactive: Due to defect and quality issues dental scanner may not scan properly/accurately
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
Catheter manufactured at the incorrect length.
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
The DxI 9000 Access Immunoassay Analyzer wash wheel mixer may not spin freely within the idler pulley housing. When the problem occurs, the analyzer may generate a system event for a Wash…
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
