Philips Azurion, Allura Xper and Eleva Systems
Summary
Contact the manufacturer if you require additional information.
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
MultiDiagnost Eleva - Image Intensifier - TV Image Detector |
Not applicable. |
70832 |
Allura Xper FD20/15 |
Not applicable. |
722058 |
Allura Xper FD10 |
Not applicable. |
ALLURA XPER FD10 |
Allura Xper FD20/20 (Product Of Alluraclarity Family) |
Not applicable. |
722038 |
Allura Xper FD20 Or Table (Product Of Alluraclarity Family) |
Not applicable. |
722035 |
Azurion 7 M20 |
Not applicable. |
722 224 |
Multidiagnost Eleva - Flat Detector - Image Detector |
Not applicable. |
70834 |
Allura Xper FD10/10 (Product Of Alluraclarity Family) |
Not applicable. |
722027 |
Allura Xper FD20 (Product Of Alluraclarity Family) |
Not applicable. |
722028 |
Allura Xper FD20/10 (Product Of Alluraclarity Family) |
Not applicable. |
722029 |
Azurion 7 B12 |
Not applicable. |
722 067 |
Azurion 7 B20 |
Not applicable. |
722 226 |
Azurion 7 M12 |
Not applicable. |
722 223 |
Issue
It was reported to Philips that after a procedure was completed, the staff began cleaning and transferring the patient to the patient's trolley. While moving the control screen (cs) monitor, one of the hose cable carriers from the monitor's cable carrier came loose and fell, striking an employee on the head. The injured employee sustained a minor concussion and was placed under observation in the hospital for the entire day before being discharged to rest at home.
Recall start date: August 23, 2024
Additional information
Details
Philips Medical Systems Nederland B.V.
Veenpluis 6, Best, Netherlands, 5684 PC
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