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

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  Reason
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  Affected products

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