International safety notice
Corrective action for ABL80 FLEX Analyzers configured with either FLEX or BASIC software, Radiometer Medical
Germany / BfArM · DEU · Feb 29, 2012
Key facts
| Title | Corrective action for ABL80 FLEX Analyzers configured with either FLEX or BASIC software, Radiometer Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ABL80 FLEX Analyzers configured with either FLEX or BASIC software, Radiometer Medical |
| Manufacturer | Corrective action for ABL80 FLEX Analyzers configured with either FLEX or BASIC software, Radiometer Medical |
| Models | QUALICHECK4, 944-055, S7450, ABL80 |
| Date | Feb 29, 2012 |
| 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