FDA Medical Device Recalls (openFDA)
Vitalgo Inc.: VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003
- Recall number
- Z-2739-2018
- Recalling firm
- Vitalgo Inc.
- Product
- VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003
- Status
- Terminated
- Initiated
- 2018-04-12
- Posted
- not on file
- Terminated
- 2019-03-12
- Reason
- Potential for unintentional movement of the support surface of the bed from tilted position to horizontal position or any position in between.
- Root cause
- Component change control
- Action
- The customer was notified of the recall on about 04/12/2018 via letter. The letter was follow up to previous communications on 02/19/2018, 03/06/2018, 03/07/2018, 03/26/2018, and 04/09/2018 and reminded the customer that all affected beds at each service center are to be placed on Quality Hold. Further directions will be provided at a later time to conduct a correction on the beds.
- Quantity
- 85 units
- Distribution
- US distribution to Texas.
- Lot, serial or model codes
- 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
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FNL
- Firm FEI
- 3010034871
- Firm city
- Fort Lauderdale
- Firm state
- FL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28