International safety notice
Venous Line Clamp Occlusion Failure on hemodialysis instruments SYSTEM 1000, TINA, AURORA and ARENA from Baxter
Germany / BfArM · DEU · Mar 10, 2006
Key facts
| Title | Venous Line Clamp Occlusion Failure on hemodialysis instruments SYSTEM 1000, TINA, AURORA and ARENA from Baxter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Venous Line Clamp Occlusion Failure on hemodialysis instruments SYSTEM 1000, TINA, AURORA and ARENA from Baxter |
| Manufacturer | Venous Line Clamp Occlusion Failure on hemodialysis instruments SYSTEM 1000, TINA, AURORA and ARENA from Baxter |
| Date | Mar 10, 2006 |
| 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