This page has been archived on the Web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.
MobileDiagnost WDR
- Starting date:
- December 17, 2012
- Posting date:
- January 7, 2013
- 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-16637
Recalled Products
- MobileDiagnost WDR
Reason
- When the operator moves an image to another view, the electronic marker might be placed at the wrong anatomical position in the resulting image.
- If by an electrical connection failure between motor speed sensor and digital motion control board or a related software defect, the movement speed regulation does not work as intended, the device may move with increasing speed and/or into a wrong direction after releasing the dead man switch (handle bar) during 1.5 seconds maximum until the brake is activated.
Affected products
A. MobileDiagnost WDR
Lot or serial number
N/A
Model or catalog number
9890 010 8952X
Companies
- Manufacturer
- Philips Medical Systems DMC GMBH