International safety notice
Recall for Ascendra Balloon Catheter, Edwards
Germany / BfArM · DEU · Aug 27, 2008
Key facts
| Title | Recall for Ascendra Balloon Catheter, Edwards |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Ascendra Balloon Catheter, Edwards |
| Manufacturer | Recall for Ascendra Balloon Catheter, Edwards |
| Models | OOBCL23, OOBCL26, OBCL23, 949.250.2500, 92614, 949.250.2525, 949.2502500, 1-949-756-4525, 250.2525 |
| Date | Aug 27, 2008 |
| 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