International safety notice
Corrective action and recall from Radiometer Medical for ABL700/800 analyzers
Germany / BfArM · DEU · Aug 19, 2005
Key facts
| Title | Corrective action and recall from Radiometer Medical for ABL700/800 analyzers |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ABL700/800 analyzers |
| Manufacturer | Corrective action and recall from Radiometer Medical for ABL700/800 analyzers |
| Models | ABL800, ABL700 |
| Date | Aug 19, 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