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Health product recall

OASIS Power Wheelchair (2015-01-29)

Starting date:
January 29, 2015
Posting date:
March 5, 2015
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-52447

Recalled Products

OASIS Power Wheelchair

Reason

A problem has been identified with the front rudder. It was found that a weld was incomplete, which may cause the rudder to break.

Affected products

OASIS Power Wheelchair

Lot or serial number

More than 10 LOTS, please contact the manufacturer.

Model or catalog number

OASIS A700 G2

Companies
Manufacturer

Orthofab Inc.

2160 De Celles

Quebec

G2C 1X8

Quebec

CANADA