Hitachi Medical Systems America Inc recalls
Every recall we track for Hitachi Medical Systems America Inc — 6 in all, from 2017–2021 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
6 recalls since 2017. 17% rated “stop using now”.
All FDA recall records for Hitachi Medical Systems America Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 1 | 0 | 0 | 1 |
| 2018 | 1 | 1 | 0 | 0 | 2 |
| 2019 | 0 | 1 | 0 | 0 | 1 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Hitachi Medical Systems America Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Hitachi Medical Systems America Inc recalls
6 shown- Lower riskMedical device
Hitachi Medical Systems America Inc recalls Ultrasonic pulsed doppler imaging system - Product Usage: intended for use by trained personnel (doctor, Sonographer,
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 MedicalMar 1, 2021 - Lower riskMedical device
Hitachi Medical Systems America Inc recalls UST-2265-2 Probe, Part Number: UST-2265-2 - Product Usage: The UST-2265-2 probe is intended to be used for diagnostic
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 MedicalJan 31, 2020 - Use cautionMedical device
Hitachi Medical Systems America Inc recalls Hitachi Scenaria Whole-body X-ray CT System
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 MedicalOct 16, 2019 - Use cautionMedical device
Hitachi Medical Systems America Inc recalls Hitachi Scenaria CT system Product Usage: The SCENARIA CT system is indicated for head, whole body, cardiac and
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.
HitachiJun 29, 2018 - Stop using nowMedical device
Hitachi Medical Systems America Inc recalls Hitachi Oasis MRI system Product Usage: Hitachi MR system is an imaging device and is intended to provide the physician
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.
HitachiJun 18, 2018 - Use cautionMedical device
Hitachi Medical Systems America Inc recalls Ultrasound Transducer, Model Number: UST-5550-R, is used in conjunction with a diagnostic ultrasound system evaluation
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.
Hitachi MedicalOct 20, 2017
Hitachi Medical Systems America Inc recall questions
How many recalls has Hitachi Medical Systems America Inc had?
6 recalls from Hitachi Medical Systems America Inc are on record with U.S. safety agencies, from 2017–2021.
What is the most recent Hitachi Medical Systems America Inc recall?
Hitachi Medical Systems America Inc recalls Ultrasonic pulsed doppler imaging system - Product Usage: intended for use by trained personnel (doctor, Sonographer,, dated Mar 1, 2021. Every Hitachi Medical Systems America Inc recall is listed on this page, newest first.
What should I do if I have a recalled Hitachi Medical Systems America Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Hitachi Medical Systems America Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.