Z-2739-2018 Class II Terminated
FDA device recall Z-2739-2018 was initiated by Vitalgo Inc. on April 12, 2018 and is designated Class II. 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. The recall status is terminated (terminated March 12, 2019). Affected quantity: 85 units.
Recall Details
- Product Type
- Devices
- Report Date
- August 15, 2018
- Initiation Date
- April 12, 2018
- Termination Date
- March 12, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 85 units
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.
Distribution Pattern
US distribution to Texas.
Code Information
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