International safety notice

Common name: General purpose ultrasound imaging device Brand name: (1) Ultrasonic diagnostic device Aplio i900 TUS-AI900 (2) Ultrasound diagnostic device Aplio i800 TUS-AI800 (3) Ultrasound diagnostic device Aplio i700 TUS-AI700 (4) Ultrasound diagnostic device Aplio a550 CUS-AA550 (5) Ultrasound diagnostic device Aplio a450 CUS-AA450 (6) Ultrasonic diagnostic device Aplio a CUS-AA000

Japan / PMDA Recalls · JPN · Jun 16, 2022

Key facts

Regulator Japan / PMDA Recalls
Country JPN
Brand Common name: General purpose ultrasound imaging device Brand name: (1) Ultrasonic diagnostic device Aplio i900 TUS-AI900 (2) Ultrasound diagnostic device Aplio i800 TUS-AI800 (3) Ultrasound diagnostic device Aplio i700 TUS-AI700 (4) Ultrasound diagnostic device Aplio a550 CUS-AA550 (5) Ultrasound diagnostic device Aplio a450 CUS-AA450 (6) Ultrasonic diagnostic device Aplio a CUS-AA000
Manufacturer Canon Medical Systems Inc.
Models 5CA2072002, TUS-AI700, 5CB2142030, 5CB2132113, 5CB2122023, J3B20Y2597, CUS-AA450, 6CC2222018, 5CB20X2020, 5CB2112077, 6CB21X2109, 5CB2122084 and 24 more
Date Jun 16, 2022
Regulator page info.pmda.go.jp

At a glance

  • No Recall
  • No Field safety notice

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

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