International safety notice
Recall for CROSSOVER™ Sheath Introducer, Cordis
Germany / BfArM · DEU · Oct 30, 2009
Key facts
| Title | Recall for CROSSOVER™ Sheath Introducer, Cordis |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | CROSSOVER™ Sheath Introducer, Cordis |
| Manufacturer | Recall for CROSSOVER™ Sheath Introducer, Cordis |
| Models | U0000051, U0000039, U0000036, U0000038, 403685S, 403645S, U0000057, 00000032, U0000042, 00000056, U0000052, 00000028 and 14 more |
| Date | Oct 30, 2009 |
| 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