FDA DeviceClass IINotable
FDA Recall: Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire
Description
Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.
Hazard
Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.
Remedy
3487 units
Related Recalls
2026-06-10 · FDA_DEVICE
FDA Recall: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine H
Becton Dickinson & Company
2026-06-10 · FDA_DEVICE
FDA Recall: BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
CareFusion 303, Inc.
2026-06-10 · FDA_DEVICE
FDA Recall: Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 an
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
2026-06-10 · FDA_DEVICE
FDA Recall: Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10
Kico Knee Innovation Company