International safety notice
220-0201
New Zealand / Medsafe Recalls · NZL · Nov 29, 2013
Key facts
| Title | 220-0201 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Bio-Rad D-10 dual Program Reorder Pack |
| Manufacturer | Bio-Rad Laboratories Inc |
| Models | 220-0201 |
| Event type | Safety Notice |
| Action type | Correction |
| Date | Nov 29, 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