International safety notice
Corrective Action for HemoCue Glucose 201 DM and HemoCue Hb 201 DM Analyzers, HemoCue AB
Germany / BfArM · DEU · Nov 9, 2010
Key facts
| Title | Corrective Action for HemoCue Glucose 201 DM and HemoCue Hb 201 DM Analyzers, HemoCue AB |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | HemoCue Glucose 201 DM and HemoCue Hb 201 DM Analyzers, HemoCue AB |
| Manufacturer | Corrective Action for HemoCue Glucose 201 DM and HemoCue Hb 201 DM Analyzers, HemoCue AB |
| Models | LLGTTI0CUE, 0MSTAENING, 41160001E, V-0021, OFT1E, VERIFIC3 |
| Date | Nov 9, 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