International safety notice
366812|366817|366822|366827|366832|366837|366842|366847
New Zealand / Medsafe Recalls · NZL · May 22, 2015
Key facts
| Title | 366812|366817|366822|366827|366832|366837|366842|366847 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Biotronik Pulsar-18 Peripheral Stent, 200mm |
| Manufacturer | Biotronik AG |
| Models | 366812, 366842, 366837, 366832, 366827, 366822, 366817, 366847 |
| Event type | Recall |
| Action type | Recall |
| Date | May 22, 2015 |
| 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