International safety notice
Recall for Avidia Angiographic Contrast Injector, Imaxeon
Germany / BfArM · DEU · Aug 17, 2010
Key facts
| Title | Recall for Avidia Angiographic Contrast Injector, Imaxeon |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Avidia Angiographic Contrast Injector, Imaxeon |
| Manufacturer | Recall for Avidia Angiographic Contrast Injector, Imaxeon |
| Models | 61-2-8845-4915, 50PSI, 4.50.8, 10MIN, 4.60.3 |
| Date | Aug 17, 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