Recall Z-1182-2017— Invacare Corporation

Class II · Terminated

Class II FDA medical device recall by Invacare Corporation, initiated 2016-12-02, terminated 2017-11-02. FDA's recall record names no specific 510(k) clearance for this event. Product: Bariatric Bed - BAR600IVC. Reason: The junction box used in the bariatric bed may emit sparks and result in a fire..

Recalling firm
Invacare Corporation
Classification
Class II
Status
Terminated
Initiated
2016-12-02
Terminated
2017-11-02
Firm location
Elyria, OH, United States

Product description

Bariatric Bed - BAR600IVC

Reason for recall

The junction box used in the bariatric bed may emit sparks and result in a fire.

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