International safety notice
816301006
New Zealand / Medsafe Recalls · NZL · Jun 19, 2015
Key facts
| Title | 816301006 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Biomet Medium Bone Plate forceps |
| Manufacturer | Biomet Trauma |
| Models | 816301006 |
| Event type | Recall |
| Action type | Recall |
| Date | Jun 19, 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