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Health product recall

I-Guide System 2.X incl. Workstation (2014-05-29)

Starting date:
May 29, 2014
Posting date:
June 18, 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-40055

Recalled Products

I-Guide System 2.X incl. Workstation 

Reason

I-Guide workflow possible despite I-Guide key in off position.

Affected products

I-Guide System 2.X incl. Workstation 

Lot or serial number

Not applicable

Model or catalog number

P10603-102

Companies
Manufacturer
Medical Intelligence Medizintechnik Gmbh
Robert-Bosch-Strasse 8
Schwabmunchen
86830
GERMANY