International safety notice
8888-160325|8888-160333|8888-160341
New Zealand / Medsafe Recalls · NZL · Sep 18, 2013
Key facts
| Title | 8888-160325|8888-160333|8888-160341 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Kendall Argyle Single Lumen Polyurethane Umbilical Vessel Catheter |
| Manufacturer | Kendall, a division of Tyco Healthcare Group LP |
| Models | 8888-160333, 8888-160341, 8888-160325 |
| Event type | Safety Notice |
| Action type | Correction |
| Date | Sep 18, 2013 |
| 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