Health product recall

Cios Alpha (2019-04-10)

Starting date:
April 10, 2019
Posting date:
April 29, 2019
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-69742

Last updated: 2019-04-30

Affected Products

Cios Alpha

Reason

Siemens is providing an optimised set of FD calibration data to prevent the possibility of black fringes appearing in seldom cases and special circumstances at the border of objects/patients to direct radiation images.

Affected products

Cios Alpha

Lot or serial number

12577

Model or catalog number

10308191

Companies
Manufacturer
Siemens Healthcare GmbH
Henkestr. 127
Erlangen
91052
GERMANY