International safety notice
Common name: General purpose ultrasound imaging device Brand name: (1) Ultrasonic diagnostic device ALOKA ARIETTA 850 (2) Ultrasonic diagnostic device ARIETTA 750 (3) Ultrasound diagnostic device ARIETTA 65 (4) Ultrasound diagnostic device ALOKA LISENDO 880
Japan / PMDA Recalls · JPN · Apr 26, 2022
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common name: General purpose ultrasound imaging device Brand name: (1) Ultrasonic diagnostic device ALOKA ARIETTA 850 (2) Ultrasonic diagnostic device ARIETTA 750 (3) Ultrasound diagnostic device ARIETTA 65 (4) Ultrasound diagnostic device ALOKA LISENDO 880 |
| Manufacturer | Fujifilm Healthcare Co., Ltd. |
| Models | G3134918, G3156289, G3138584, G3156145, G3160833, G3138600, G3156417, G3162247, G3151942, G3156290, G3151905, G3085660 and 655 more |
| Date | Apr 26, 2022 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1