FujiFilm Healthcare Americas Corporation recalls Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3
Diagnostic ultrasound system with the specified software version and used in conjunction with a Fujifilm (formally Hitachi) transducer does not display the measurement results correctly with two cardiology measurement…
Read the official notice →- Date
- 2021-11-10
- Country
- United States
- Brand
- FUJIFILM Healthcare Americas
- Product
- Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3
- Classification
- Class II
- Units
- Nationwide
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
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General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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