Health product recall

Oasis Power Wheelchair (2017-09-21)

Starting date:
September 21, 2017
Posting date:
May 31, 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-70059



Last updated: 2019-05-31

Affected Products

Oasis Power Wheelchair

Reason

An engineering change (DCI-3322) was made to the defective part, which consists of adding solder to the parts of the defective part that did not contain it and thus improving its resistance. In addition, a chamfer has been added to increase the weld contact area. Finally, at each batch manufactured, a destructive test will be performed.

Affected products

Oasis Power Wheelchair

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number
  • PC
  • PP
Companies
Manufacturer

Orthofab Inc.

2160 De Celles

Quebec

G2C 1X8

Quebec

CANADA