International safety notice
Corrective action for Synchron LX20, LX20 Pro and LXi725 Clinical Systems, Beckman Coulter
Germany / BfArM · DEU · May 27, 2011
Key facts
| Title | Corrective action for Synchron LX20, LX20 Pro and LXi725 Clinical Systems, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Synchron LX20, LX20 Pro and LXi725 Clinical Systems, Beckman Coulter |
| Manufacturer | Corrective action for Synchron LX20, LX20 Pro and LXi725 Clinical Systems, Beckman Coulter |
| Models | B06649, A96677, A93901, 664090, A35895AB, 389227, A32319 |
| Date | May 27, 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