International safety notice
Recall of the Arctic Circler® Linear Cardiac Cryoablation Catheter from CryoCath Technologies
Germany / BfArM · DEU · Aug 23, 2006
Key facts
| Title | Recall of the Arctic Circler® Linear Cardiac Cryoablation Catheter from CryoCath Technologies |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the Arctic Circler® Linear Cardiac Cryoablation Catheter from CryoCath Technologies |
| Manufacturer | Recall of the Arctic Circler® Linear Cardiac Cryoablation Catheter from CryoCath Technologies |
| Models | 2AC30, 50327, 011-514-694-1212, 16771, 011-514-694-6279, 1-514-694-1212, 6946279, 50312, CRYOCATH16771, 50103, 00486, 00035 and 2 more |
| Date | Aug 23, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 100–999 Matching catalog numbers 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