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Health product recall

Mobilediagnost WDR (2014-08-20)

Starting date:
August 20, 2014
Posting date:
September 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-41261

Mobilediagnost WDR

Reason

Philips has become aware that if the system drives over insulated flooring or carpeting and then over an uninsulated, electrically grounded section, an electrostatic discharge can cause the system's digital motion control (DMC) board to malfunction, resulting in unintended movement of the system, e.g., an increase in speed or a change of direction.

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