International safety notice
Corrective Action of Abbott for Architect B12
Germany / BfArM · DEU · Dec 27, 2004
Key facts
| Title | Corrective Action of Abbott for Architect B12 |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Architect B12 |
| Manufacturer | Corrective Action of Abbott for Architect B12 |
| Models | 13DEC2004, 609-20, 6C21-32, 6C09-20, I2000SR, 6C21-22, 6C21-27, I2000, 6C09-25, 3DEC2004 |
| Date | Dec 27, 2004 |
| Regulator page | bfarm.de |
At a glance
- No 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