International safety notice
Recall for Architect Pre-Trigger Solution, Abbott
Germany / BfArM · DEU · Sep 20, 2010
Key facts
| Title | Recall for Architect Pre-Trigger Solution, Abbott |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Architect Pre-Trigger Solution, Abbott |
| Manufacturer | Recall for Architect Pre-Trigger Solution, Abbott |
| Models | 87479LF00, FA20AUG2010, 87573LF00, 88615LF00, 87164LF00, 90499LF00, 90291LF00, 6E23-65 |
| Date | Sep 20, 2010 |
| 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