International safety notice
Recall for Logicath 12 F Haemodialysis Central Venous Catheters, Smiths Medical
Germany / BfArM · DEU · Oct 11, 2011
Key facts
| Title | Recall for Logicath 12 F Haemodialysis Central Venous Catheters, Smiths Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Logicath 12 F Haemodialysis Central Venous Catheters, Smiths Medical |
| Manufacturer | Recall for Logicath 12 F Haemodialysis Central Venous Catheters, Smiths Medical |
| Models | 242959, 85630, 242959-310 |
| Date | Oct 11, 2011 |
| 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