International safety notice
Corrective action for the Ingenia, Intera, Achieva and Achieva MR systems on R5.1.1 and R5.1.2 with the MobiView software option, Philips Healthcare
Germany / BfArM · DEU · Jul 9, 2014
Key facts
| Title | Corrective action for the Ingenia, Intera, Achieva and Achieva MR systems on R5.1.1 and R5.1.2 with the MobiView software option, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Ingenia, Intera, Achieva and Achieva MR systems on R5.1.1 and R5.1.2 with the MobiView software option, Philips Healthcare |
| Manufacturer | Corrective action for the Ingenia, Intera, Achieva and Achieva MR systems on R5.1.1 and R5.1.2 with the MobiView software option, Philips Healthcare |
| Models | 00431, 00426, R5.1.2, FCO781, FSN781, R5.1.7, R5.1.1 |
| Date | Jul 9, 2014 |
| 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