International safety notice
AGA Medical Corporation recalls AMPLATZER® Delivery Systems and AMPLATZER® Exchange Systems
Germany / BfArM · DEU · Jan 25, 2005
Key facts
| Title | AGA Medical Corporation recalls AMPLATZER® Delivery Systems and AMPLATZER® Exchange Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | AGA Medical Corporation recalls AMPLATZER® Delivery Systems and AMPLATZER® Exchange Systems |
| Manufacturer | AGA Medical Corporation recalls AMPLATZER® Delivery Systems and AMPLATZER® Exchange Systems |
| Models | 1-763-513-9226, 763513-9226, 55427, 1-763-513-9227 |
| Date | Jan 25, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
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