Every recall we track for Invivo Corporation — 9 in all — plus the complaints and injury reports the public filed about them.
Invivo Corporation recalls MR Coils with mistakenly printed IPX1 water rating labels. These coils are used with MRI scanners. Affected models include dS Knee Sch 1.5T, dS Shoulder Sch 3.0T, and others. No action is required as the labels are incorrect but not dangerous.
Invivo recalls specific MRI monitor models due to insufficient shielding of Philips SensaVue DVI Adapter, which may cause interference with MRI safety systems.
Invivo recalls Xper Flex Cardio Physiomonitoring System software version 1.6.0.0388 due to potential freezing of invasive blood pressure readings during certain actions. Affected units have specific serial numbers listed in the recall notice.
Invivo recalls Xper Flex Cardio Physiomonitoring System with faulty software version 1.6.0.0388 that may cause inaccurate ECG readings and heart rate displays. Affected units have specific serial numbers listed in the recall.
US1433000052
Invivo recalls DynaCad software updates 3.5 causing incorrect pharmacokinetic and diffusion maps. Users may underestimate critical medical values. No remedy stated.
Invivo recalls Xper Flex Cardio Physiomonitoring System units with specific serial numbers due to a potential issue where pressing ESC key accidentally closes Full Disclosure Control Window during playback.
