International safety notice
Field Safety Corrective Action for the OctoNova Hemofiltration Device, Nikkiso Europe GmbH
Germany / BfArM · DEU · Jul 26, 2012
Key facts
| Title | Field Safety Corrective Action for the OctoNova Hemofiltration Device, Nikkiso Europe GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the OctoNova Hemofiltration Device, Nikkiso Europe GmbH |
| Manufacturer | Field Safety Corrective Action for the OctoNova Hemofiltration Device, Nikkiso Europe GmbH |
| Models | FCA.NE.07, 30855, GE.F090-00, GE.F090.OO, GE-F076-OO, FCANE07, GE-F076, 2012-06-29, GE-F091.OO, FCA-NE-07, 4.30.XX, D-30855 and 4 more |
| Date | Jul 26, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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