Every recall we track for Hitachi Medical Systems America Inc — 6 in all — plus the complaints and injury reports the public filed about them.
Hitachi Medical recalls Arietta 850 ultrasound software versions 4.0.0-4.0.2 with focus errors that may exceed regulatory acoustic limits when used with C252 probes.
Hitachi Medical recalls 18 specific UST-2265-2 ultrasound probes due to potential miswiring in inner cables, which may cause lower peak velocity readings during diagnostic imaging. Affected units have unique serial numbers.
Hitachi Medical recalls Scenaria whole-body X-ray CT systems (S5002-S5014, S5017-S5:5044) due to potential cable detachment during scans. Affected units may eject cables, causing safety risks.
Hitachi recalls Scenaria CT systems after reports of table failing to stop during patient positioning, risking injury or equipment damage. Affected units may need safety updates.
Hitachi Medical recalls Oasis MRI systems with exposed stainless steel belt that can cause finger cuts during use. Affected models M001-M028, M030-M108, M110-M266, M951, M9:152. Stop using immediately to prevent finger injuries.
Hitachi Medical recalls UST-5550-R ultrasound transducers used in surgical procedures due to risk of electrical shock. Affected units may cause injury during medical procedures.
