Recall Z-2739-2018— Vitalgo Inc.

Class II · Terminated

Class II FDA medical device recall by Vitalgo Inc., initiated 2018-04-12, terminated 2019-03-12. FDA's recall record names no specific 510(k) clearance for this event. Product: VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003. Reason: Potential for unintentional movement of the support surface of the bed from tilted position to horizontal position or any position in between..

Recalling firm
Vitalgo Inc.
Classification
Class II
Status
Terminated
Initiated
2018-04-12
Terminated
2019-03-12
Firm location
Fort Lauderdale, FL, United States

Product description

VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003

Reason for recall

Potential for unintentional movement of the support surface of the bed from tilted position to horizontal position or any position in between.

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