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Health product recall

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