Recall Z-1036-2015— Invacare Corporation

Class II · Terminated

Class II FDA medical device recall by Invacare Corporation, initiated 2014-12-05, terminated 2015-06-18. FDA's recall record names no specific 510(k) clearance for this event. Product: G- Series Beds; G29 full length bed rails assembly. Reason: Invacare identified that the rail mounting bracket on the G29 full length bed rail was out of specification for entrapment safety..

Recalling firm
Invacare Corporation
Classification
Class II
Status
Terminated
Initiated
2014-12-05
Terminated
2015-06-18
Firm location
Elyria, OH, United States

Product description

G- Series Beds; G29 full length bed rails assembly

Reason for recall

Invacare identified that the rail mounting bracket on the G29 full length bed rail was out of specification for entrapment safety.

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