Health product recall

Azurion 7 M12, M20 (2019-07-05)

Starting date:
July 5, 2019
Posting date:
July 19, 2019
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-70481



Last updated: 2019-07-19

Affected Products

A. Azurion 7 M12

B. Azurion 7 M20

Reason

The cold restart of Azurion R1.2 Systems may take up to 7 minutes if the system is connected to the mains power supply for more than 50 days.

 

Affected products

A. Azurion 7 M12

Lot or serial number

Not applicable. 

Model or catalog number

722 078

Companies
Manufacturer

Philips Medical Systems Nederland B.V.

Veenpluis 4-6

Best

5684 PC

NETHERLANDS


B. Azurion 7 M20

Lot or serial number

Not applicable. 

Model or catalog number

722 079

Companies
Manufacturer

Philips Medical Systems Nederland B.V.

Veenpluis 4-6

Best

5684 PC

NETHERLANDS