International safety notice
A voluntary recall was implemented because some raw materials were changed and an accessory (flex tube) that was different from the approved items was shipped. I will.
Japan / PMDA Recalls · JPN · Jun 3, 2024
Key facts
| Title | A voluntary recall was implemented because some raw materials were changed and an accessory (flex tube) that was different from the approved items was shipped. I will. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common Name: Single Use Artificial Nasal Filter Brand name: Artificial nose with bacterial filter |
| Manufacturer | Air Life Japan LLC |
| Models | 0209385, 557033300 |
| Date | Jun 3, 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