Voyager Duo Lift (2019-01-26)

Starting date:

January 26, 2019

Posting date:

February 15, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-69032

Last updated: 2020-02-04

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  Reason
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  Affected products

Affected Products

Voyager Duo Lift 

Reason

During final testing on the production line, it was observed by assemblers that the fuse of the printed circuit board (PCB) for Voyager Duo Ceiling Lift was blowing, which could lead eventually to interruption in the up-down motion of the device.

Affected products