International safety notice
AMB412351000|AMB412371000|AMB412391000|AMB412411000
New Zealand / Medsafe Recalls · NZL · Jun 30, 2022
Key facts
| Title | AMB412351000|AMB412371000|AMB412391000|AMB412411000 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Vivasight 2 |
| Manufacturer | Ambu AS |
| Models | AMB412411000, AMB412391000, AMB412351000, AMB412371000 |
| Event type | Recall |
| Action type | Recall |
| Date | Jun 30, 2022 |
| Regulator page | medsafe.govt.nz |
At a glance
- Yes 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