International safety notice
Corrective action for the Manual Collimator Exchange system in use with an ADAC Vertex Plus, CARDIO, Solus or Vertex V60 imaging system, Philips Healthcare
Germany / BfArM · DEU · Apr 15, 2015
Key facts
| Title | Corrective action for the Manual Collimator Exchange system in use with an ADAC Vertex Plus, CARDIO, Solus or Vertex V60 imaging system, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Manual Collimator Exchange system in use with an ADAC Vertex Plus, CARDIO, Solus or Vertex V60 imaging system, Philips Healthcare |
| Manufacturer | Corrective action for the Manual Collimator Exchange system in use with an ADAC Vertex Plus, CARDIO, Solus or Vertex V60 imaging system, Philips Healthcare |
| Models | 88200484 |
| Date | Apr 15, 2015 |
| 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