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Health product recall

Fuze

Starting date:
August 2, 2012
Posting date:
September 17, 2012
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices, Product Safety
Audience:
General Public (GP), Healthcare Professionals, Hospitals
Identification number:
RA-15560

Recalled Products

A. Fuze

Reason

The hex bolts could shear and cause the axle plate or pivot arm to detach and in turn could cause the chair to collapse when someone sits on it.

Affected products

A. Fuze

Lot or serial number

52651 to 52919

Model or catalog number

Fuze 20, Fuze 50

Companies
Manufacturer
PDG Product Design Group Inc.