International safety notice
Recall of affected lots of the coronay stent “Cypher Select ™+“, Cordis
Germany / BfArM · DEU · Jun 19, 2009
Key facts
| Title | Recall of affected lots of the coronay stent “Cypher Select ™+“, Cordis |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of affected lots of the coronay stent “Cypher Select ™+“, Cordis |
| Manufacturer | Recall of affected lots of the coronay stent “Cypher Select ™+“, Cordis |
| Models | 43466688, 14037590, CRB13250, CRB33300, 4-277, 14081555, 14045692, 14050422, 14061699, 14033114, 14091346, 14030210 and 356 more |
| Date | Jun 19, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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