International safety notice

Common name: Stationary digital general-purpose X-ray fluoroscopic diagnostic device (dual energy bone X-ray absorptiometry device) Sales name: X-ray television system SONIALVISION G4

Japan / PMDA Recalls · JPN · Nov 21, 2023

Key facts

Regulator Japan / PMDA Recalls
Country JPN
Brand Common name: Stationary digital general-purpose X-ray fluoroscopic diagnostic device (dual energy bone X-ray absorptiometry device) Sales name: X-ray television system SONIALVISION G4
Manufacturer Shimadzu Corporation
Models 41C353DD8001, 41C353DD9001, 41C353DC9001, 41C353DD3002, 41C355BD2001, 41C353DD2002, 41C3508C8003, 41C353DD2001, 41C353DD6002, 41C3526C9001, 41C353DC8005, 41C355BCC002 and 21 more
Date Nov 21, 2023
Regulator page info.pmda.go.jp

At a glance

  • No Recall
  • No Field safety notice

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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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