International safety notice
Corrective action of the RD/Hitachi 902/904/911/912, RD Hitachi/917 Modular P and Modular P for the test glucose in haemolysate from Roche
Germany / BfArM · DEU · Sep 13, 2007
Key facts
| Title | Corrective action of the RD/Hitachi 902/904/911/912, RD Hitachi/917 Modular P and Modular P for the test glucose in haemolysate from Roche |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the test glucose in haemolysate from Roche |
| Manufacturer | Corrective action of the RD/Hitachi 902/904/911/912, RD Hitachi/917 Modular P and Modular P for the test glucose in haemolysate from Roche |
| Models | 759-4747, 11447521, GLU2H, 11929542, 11447513, MESSBEREICH4, 11929534, 63-750, 11876899, 20767131 |
| Date | Sep 13, 2007 |
| 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