International safety notice

It has been discovered that products sterilized at a manufacturing facility other than the registered sterilization manufacturing facility were being shipped together. Ta. vinegar.

Japan / PMDA Recalls · JPN · Dec 10, 2024

Key facts

Title It has been discovered that products sterilized at a manufacturing facility other than the registered sterilization manufacturing facility were being shipped together. Ta. vinegar.
Regulator Japan / PMDA Recalls
Country JPN
Brand Common name: Active instruments for radiofrequency treatment Sales name: Monopolar
Manufacturer Gunze Medical Co., Ltd.
Models ES54-B, 0323U, ES10-B, ES37-B, A805-B, ES20-B, ES01-B, ES38-B, ES46-B, ES12-B, ES09-B, ES07-B and 6 more
Date Dec 10, 2024
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

Browse all International device safety notices