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Health product recall

Artis Zeego System

Starting date:
November 14, 2012
Posting date:
December 10, 2012
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public (GP), Healthcare Professionals, Hospitals
Identification number:
RA-16307

Reason

In case of an unlikely failure of a brake, the C-Arm of the system may descend on the patient or operator. The risk of a failure of the brake and the associated potential hazard for patients or operators is specific for the stated software versions (VC14, VC20 or VC21) in conjunction with a specific configuration for the Artis Zeego system.

Affected products

A. Artis Zeego System

Lot or serial number

160423, 160810

 

Model or catalog number

10280959

Companies

Manufacturer

Siemens AG