Health product recall

Mobilediagnost WDR (2018-06-01)

Starting date:
June 1, 2018
Posting date:
June 14, 2018
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-67048

Affected products

Mobilediagnost WDR

Reason

Philips has become aware when the operator or a bystander touches the area of the inner part of the vertical sliding column (on which the tube arm moves up or down), without paying attention of the tube arm movement, the fingers can be pinched.

Affected products

Mobilediagnost WDR

Lot or serial number

Not applicable

Model or catalog number

9890 010 8952X

Companies
Manufacturer
Philips Medical Systems DMC GmbH
Rontgenstrabe 24
Hamburg
22335
GERMANY