International safety notice
E-BFV01M|E-BFV01M05
New Zealand / Medsafe Recalls · NZL · Oct 25, 2013
Key facts
| Title | E-BFV01M|E-BFV01M05 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Panbio Barmah Forest VirusIgM Elisa 86 tests/ 480 Tests |
| Manufacturer | Inverness Medical Innovations Australia Pty Ltd t/a Alere |
| Models | E-BFV01M, E-BFV01M05 |
| Event type | Recall |
| Action type | Recall |
| Date | Oct 25, 2013 |
| 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