International safety notice
Corrective Action for Synchron CX4/5/7 CE, CX4/5/7 Delta and CX9 ALX Clinical Systems, Beckman Coulter
Germany / BfArM · DEU · Nov 10, 2010
Key facts
| Title | Corrective Action for Synchron CX4/5/7 CE, CX4/5/7 Delta and CX9 ALX Clinical Systems, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Synchron CX4/5/7 CE, CX4/5/7 Delta and CX9 ALX Clinical Systems, Beckman Coulter |
| Manufacturer | Corrective Action for Synchron CX4/5/7 CE, CX4/5/7 Delta and CX9 ALX Clinical Systems, Beckman Coulter |
| Models | CZ99L-VOD, 993-5321, 92822-8000, LPEON-LENUEWE6PUVEO, 9614234, 369MM0, •SE6PUUEO一U96E9」PEPEOL, …一40WNTU, FCA-14523, 一01…E6ESN, XOWE.10一UEQM, 413740 and 2 more |
| Date | Nov 10, 2010 |
| 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