FDA Device recall Z-2739-2018

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

FDA Device
Class II
terminated
Published 2018-08-15

On 2018-08-15 the FDA classified a Class II recall of VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003 by Vitalgo, citing potential for unintentional movement of the support surface of the bed from tilted position to horizontal position or any position in between.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2739-2018
Classification	Class II
Status	terminated
Initiated	2018-04-12
Published	2018-08-15
Last updated	2026-09-13 11:54 UTC
Company	Vitalgo
Distribution	TX

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.

Identifiers

code_info	Model Number TLB425T-TQR; Serial Number A612, A617, A622, A629, A650, A651, A655, A657, A690, A742, A773, A791, A792, A… Model Number TLB425T-TQR; Serial Number A612, A617, A622, A629, A650, A651, A655, A657, A690, A742, A773, A791, A792, A793, A794, A603, A615, A621, A668, A673, A785, A786, A787, A788, A789, A790, A678, A679, A680, A682, A684, A685, A774, A795, A796, A798, A799, A800, A801, A802, A803, A804, A805, A806, A807, A808, A809, A810, A811, A812, A813, A814, A815, A816, A817, A818, A819, A820, A821, A822, A823, A824, A825, A826, A827, A828, A829, A831, A832, A833, A834, A835, A836, A837, A842, A843, A844, A845, A846, A847, A848, A849, A850, A851, A852

code_info

Model Number TLB425T-TQR; Serial Number A612, A617, A622, A629, A650, A651, A655, A657, A690, A742, A773, A791, A792, A…

Model Number TLB425T-TQR; Serial Number A612, A617, A622, A629, A650, A651, A655, A657, A690, A742, A773, A791, A792, A793, A794, A603, A615, A621, A668, A673, A785, A786, A787, A788, A789, A790, A678, A679, A680, A682, A684, A685, A774, A795, A796, A798, A799, A800, A801, A802, A803, A804, A805, A806, A807, A808, A809, A810, A811, A812, A813, A814, A815, A816, A817, A818, A819, A820, A821, A822, A823, A824, A825, A826, A827, A828, A829, A831, A832, A833, A834, A835, A836, A837, A842, A843, A844, A845, A846, A847, A848, A849, A850, A851, A852

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2739-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.