This page has been archived on the Web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 (2014-06-17)
- Starting date:
- June 17, 2014
- Posting date:
- July 3, 2014
- 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-40295
Recalled Products
Mobilediagnost WDR
Reason
Philips has become aware that under specific error conditions the system executes an unintended movement such as operator requests movement by presssing the dead man handle switch and pushing or pulling the handle bar.
Affected products
Mobilediagnost WDR
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
9890 010 8952X
Companies
- Manufacturer
-
Philips Medical Systems DMC GmbH
Rontgenstrabe 24
Hamburg
22335
GERMANY