International safety notice
Corrective action and recall for potassium electrodes of the analyzers Hitachi (type 902, 911, 912, 917), Modular P, Modular D and of the Cobas C series (Cobas c 501) of the manufacturer Roche.
Germany / BfArM · DEU · Aug 2, 2006
Key facts
| Title | Corrective action and recall for potassium electrodes of the analyzers Hitachi (type 902, 911, 912, 917), Modular P, Modular D and of the Cobas C series (Cobas c 501) of the manufacturer Roche. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | potassium electrodes of the analyzers Hitachi (type 902, 911, 912, 917), Modular P, Modular D and of the Cobas C series (Cobas c 501) of the manufacturer Roche. |
| Manufacturer | Corrective action and recall for potassium electrodes of the analyzers Hitachi (type 902, 911, 912, 917), Modular P, Modular D and of the Cobas C series (Cobas c 501) of the manufacturer Roche. |
| Models | 11551230, 11551213, L80XX, 10825441001, 11551221, L79XX, 11445642, 11445669, L33XX, 04522320, 03338207, 1551248 and 4 more |
| Date | Aug 2, 2006 |
| 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