International safety notice
ETHICON recalls the Portaccess 100 cm, Endoclamp Aortic Catheter
Germany / BfArM · DEU · Apr 27, 2005
Key facts
| Title | ETHICON recalls the Portaccess 100 cm, Endoclamp Aortic Catheter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ETHICON recalls the Portaccess 100 cm, Endoclamp Aortic Catheter |
| Manufacturer | ETHICON recalls the Portaccess 100 cm, Endoclamp Aortic Catheter |
| Models | 13-APR-2ØØ5, 52207243 |
| Date | Apr 27, 2005 |
| 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