Device recall: Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- When
- · day precision
- Where
- Best, NL
- Category
- recall · device_recall
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
Involved actors & entities
People, organizations and places machine-extracted from the source reporting — they power search and the correlation graph. Extracted automatically, so they can include noise, especially on events still marked unverified.
Sources
Defaxon links out to the original reporting and never republishes article text.
Correlated events
Computed by the Defaxon correlation engine — linked by shared actors, co-location, and temporal proximity. Scored hypotheses, never causal claims.
No correlated events found in the current window. As more events arrive, connections form automatically.