International safety notice
NK012.10S|NK012.S
New Zealand / Medsafe Recalls · NZL · Dec 3, 2013
Key facts
| Title | NK012.10S|NK012.S |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | The Binding Site Group Human IgM kit for use on SPA Plus |
| Manufacturer | The Binding Site Group Ltd |
| Models | NK012.10S, NK012.S |
| Event type | Safety Notice |
| Action type | Correction |
| Date | Dec 3, 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