International safety notice
Corrective action and recall of Sysmex and Dade Behring for Sysmex CA-1500, CA-7000 and CA-500 instruments
Germany / BfArM · DEU · Aug 11, 2005
Key facts
| Title | Corrective action and recall of Sysmex and Dade Behring for Sysmex CA-1500, CA-7000 and CA-500 instruments |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Sysmex CA-1500, CA-7000 and CA-500 instruments |
| Manufacturer | Corrective action and recall of Sysmex and Dade Behring for Sysmex CA-1500, CA-7000 and CA-500 instruments |
| Models | E0.-0, CA-7000, CA-550, CA-50, CA-1500, CA-500 |
| Date | Aug 11, 2005 |
| 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