Recall Z-1183-2017— 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 - BARPKG-IVC 1633. Reason: A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into 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 - BARPKG-IVC 1633

Reason for recall

A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.

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