Recall Z-0556-2013— Invacare Corporation

Class II · Terminated

Class II FDA medical device recall by Invacare Corporation, initiated 2012-11-06, terminated 2013-08-20. FDA's recall record names no specific 510(k) clearance for this event. Product: Invacare Height Adjustable (walking) Canes, Model Numbers: 8916, 8917, and 40918-6. The device is packaged six (6) canes per shipping carton. The cane is used as an aid in walking or ambulation.. Reason: Following their receipt of several customer complaints, Invacare recalled their height adjustable walking canes. The device was recalled from distribution based on reports indicating that there is a possibility that the button which holds the cane at the desired height, may suddenly and unexpectedly compress, causing the cane to collapse and cause possible injury to the user..

Recalling firm
Invacare Corporation
Classification
Class II
Status
Terminated
Initiated
2012-11-06
Terminated
2013-08-20
Firm location
Elyria, OH, United States

Product description

Invacare Height Adjustable (walking) Canes, Model Numbers: 8916, 8917, and 40918-6. The device is packaged six (6) canes per shipping carton. The cane is used as an aid in walking or ambulation.

Reason for recall

Following their receipt of several customer complaints, Invacare recalled their height adjustable walking canes. The device was recalled from distribution based on reports indicating that there is a possibility that the button which holds the cane at the desired height, may suddenly and unexpectedly compress, causing the cane to collapse and cause possible injury to the user.

Data sourced from openFDA. This site is unofficial and independent of the FDA.