Every recall we track for Medtronic Navigation, Inc.-Littleton — 17 in all — plus the complaints and injury reports the public filed about them.
Medtronic recalls O-arm O2 Imaging System mobile x-ray devices for potential image guidance failure during surgery, risking delays, extra imaging, or incomplete procedures. Affected units have specific serial numbers and product codes.
Medtronic recalls O-arm O2 Imaging Systems with incorrectly installed ground cables. This mobile x-ray system for adult/pediatric patients may pose electrical safety risks if used improperly.
Medtronic recalls specific O-arm O2 Imaging Systems due to a potential gantry belt loosening that could cause 3D images to rotate relative to patient position. Affected units have unique serial numbers and product codes.
Medtronic recalls 0-arm TM 1000 Imaging Systems with serial numbers Bl-700-00027-XXX and B1-700-00028-XXX where XXX indicates system voltage. If the charger board is faulty, the system may not take X-rays or move properly, affecting surgery.
Medtronic Navigation recalls OARM BI70002000 SYS IMAGING 02 imaging systems for a software update to prevent potential safety issues. Affected units have serial numbers C0875 to C2012.
Medtronic recalls O-arm 1000 2nd Edition Imaging Systems with software anomalies affecting startup, shutdown, communication, motion control, and image acquisition. Software update 3.1.7 will fix these issues.
Medtronic recalls O-arm 1000 2nd Edition Imaging Systems with software anomalies affecting startup, shutdown, communication, motion control, and imaging functions. Software update 3.1.7 will resolve issues.
Medtronic recalls O-arm 1000 2nd Edition Imaging Systems due to software anomalies affecting startup, shutdown, communication, motion control, and imaging functions. Update to software version 3.1.7 resolves the issue.
Medtronic recalls O-arm 1000 2nd Edition Imaging Systems with software anomalies affecting startup, shutdown, communication, motion control, and imaging. Update to software version 3.1.7 to resolve issues.
Medtronic recalls O-arm 1000 2nd Edition Imaging Systems due to software issues affecting startup, shutdown, communication, motion control, and image acquisition. Update to software version 3.1.7 resolves the problem.
Medtronic recalls O-arm 1000 2nd Edition Imaging Systems due to software issues affecting startup, shutdown, communication, motion control, and image acquisition. Affected units may require software update to version 3.1.7.
Medtronic recalls O-arm 1000 2nd Edition Imaging Systems with software anomalies affecting startup, shutdown, communication, motion control, and imaging functions. Update to software version 3.1.7 resolves the issue.
Medtronic recalls O-arm 1000 2nd Edition Imaging Systems with software anomalies affecting startup, shutdown, and imaging functions. Update to software version 3.1.7 resolves issues.
Medtronic recalls O-arm 1000 2nd Edition Imaging Systems due to software anomalies affecting startup, shutdown, communication, motion control, and imaging functions. Software update 3.1.7 will resolve issues.
Medtronic recalls O-arm 1000 2nd Edition Imaging Systems with software anomalies affecting startup, shutdown, communication, motion control, and imaging functions. Update to software version 3.1.7 resolves the issue.
Medtronic recalls O-arm 1000 mobile x-ray systems with specific model numbers for software update to fix power shutdown and image reconstruction problems.
