International safety notice
Corrective action for the HemoCue Glucose RT system and the Hemocue Glucose 201 DM RT system, HemoCue
Germany / BfArM · DEU · Mar 31, 2011
Key facts
| Title | Corrective action for the HemoCue Glucose RT system and the Hemocue Glucose 201 DM RT system, HemoCue |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the HemoCue Glucose RT system and the Hemocue Glucose 201 DM RT system, HemoCue |
| Manufacturer | Corrective action for the HemoCue Glucose RT system and the Hemocue Glucose 201 DM RT system, HemoCue |
| Models | 2011-02-22, SE-262, SE556342927201 |
| Date | Mar 31, 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