This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
Digital Diagnost
- Starting date:
- November 2, 2012
- Posting date:
- November 26, 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-15913
Recalled Products
- Digital Diagnost
Reason
When the operator for a wall stand view selects an "image rotation" different from default, or such image rotation is present in the examination database, the resulting image may be rotated in the wrong direction. When the operator manually rotates the image back, electronic side markers (if programmed) are rotated also and as a result may be placed in a wrong potition inside the image.
Affected products
A. Digital Diagnost
Lot or serial number
Not Applicable
Model or catalog number
9890 010 8390X
Companies
- Manufacturer
- Philips Medical Systems DMC GMBH