International safety notice
IAB-05830-LWS|IAB-05830-U|IAB-05840-LWS|IAB-05840-U|IAB-06830-U|IAB-06840-U|IAK-06845
New Zealand / Medsafe Recalls · NZL · Mar 4, 2016
Key facts
| Title | IAB-05830-LWS|IAB-05830-U|IAB-05840-LWS|IAB-05840-U|IAB-06830-U|IAB-06840-U|IAK-06845 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Arrow Teleflex Intra-Aortic Balloon Pump Catheter Kits and Percutaneous Insertion Kits |
| Manufacturer | Arrow International Inc |
| Models | IAB-06840-U, IAB-05830-LWS, IAB-05830-U, IAB-05840-LWS, IAB-05840-U, IAB-06830-U, IAK-06845 |
| Event type | Recall |
| Action type | Recall |
| Date | Mar 4, 2016 |
| 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