International safety notice
80063UN01|80263UN01|80263UN01-G|9002MED01|9002MED01-G
New Zealand / Medsafe Recalls · NZL · Nov 23, 2012
Key facts
| Title | 80063UN01|80263UN01|80263UN01-G|9002MED01|9002MED01-G |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | CareFusion Alaris GP Infusion System |
| Manufacturer | CareFusion Switzerland 317 Sarl |
| Models | 9002MED01, 9002MED01-G, 80263UN01, 80063UN01, 80263UN01-G |
| Event type | Safety Notice |
| Action type | Correction |
| Date | Nov 23, 2012 |
| Regulator page | medsafe.govt.nz |
At a glance
- No Recall
- Yes 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