International safety notice
Recalls of the pre-shaped neurovascular PRAWLER® und PRAWLER® SELECT™ Infusion Catheters from Cordis Neurovascular
Germany / BfArM · DEU · Aug 22, 2006
Key facts
| Title | Recalls of the pre-shaped neurovascular PRAWLER® und PRAWLER® SELECT™ Infusion Catheters from Cordis Neurovascular |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recalls of the pre-shaped neurovascular PRAWLER® und PRAWLER® SELECT™ Infusion Catheters from Cordis Neurovascular |
| Manufacturer | Recalls of the pre-shaped neurovascular PRAWLER® und PRAWLER® SELECT™ Infusion Catheters from Cordis Neurovascular |
| Models | 606S152FX, 606151, 13082015, 13090974, 13090976, 13009595, 606S155MX, 13090990, 13095822, 606S255MX, 6062310F, 13010913 and 38 more |
| Date | Aug 22, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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