Philips Healthcare recalls Azurion systems with software release R2.0.x
In the Azurion system, the user can add a new study to a patient by selecting the option "Add Study". The Add Study dialogue box is then displayed where the Patient Type is selected to perform the study. Due to a…
Read the official notice →- Date
- 2022-03-30
- Country
- United States
- Brand
- Philips Healthcare
- Product
- Azurion systems with software release R2.0.x
- Classification
- Class II
- Units
- US Nationwide Distribution
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
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General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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