International safety notice
Safety Notice for AXIS and IRIX SPECT Systems, Philips
Germany / BfArM · DEU · Jan 5, 2012
Key facts
| Title | Safety Notice for AXIS and IRIX SPECT Systems, Philips |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | AXIS and IRIX SPECT Systems, Philips |
| Manufacturer | Safety Notice for AXIS and IRIX SPECT Systems, Philips |
| Models | 88200414, 29-JUN-2011, 1-800722-9377, CNT-07310543, CNT.073105-03 |
| Date | Jan 5, 2012 |
| 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