International safety notice
Corrective action and Recall for Omni S system versions 2, 4 and 6 with CO-oximetry, Roche
Germany / BfArM · DEU · Jan 10, 2006
Key facts
| Title | Corrective action and Recall for Omni S system versions 2, 4 and 6 with CO-oximetry, Roche |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Omni S system versions 2, 4 and 6 with CO-oximetry, Roche |
| Manufacturer | Corrective action and Recall for Omni S system versions 2, 4 and 6 with CO-oximetry, Roche |
| Models | 12345, 7343383, 123457, 759-2890, D-6B305 |
| Date | Jan 10, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
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