CLASS II Device recall · Reported 15 Aug 2018 · FDA Enforcement Report
Total Lift Bed VG-TLB425T-TQR recalled by Vitalgo
Vitalgo is recalling Total Lift Bed VG-TLB425T-TQR, distributed in Texas. The recall was initiated on 12 Apr 2018 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2739-2018
- FDA event ID
- 80495
- Recalling firm
- Vitalgo, Fort Lauderdale, FL
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 12 Apr 2018
- FDA classified
- 9 Aug 2018
- Reported
- 15 Aug 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 12 Apr 2018 | Recall initiated by company | |
| 9 Aug 2018 | Classified by FDA | +119 days |
| 15 Aug 2018 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Product as listed by the FDA
VitalGo Total Lift Bed VG-TLB425T-TQR, Version 71064V0-27003
Where it was distributed
US distribution to Texas.
Questions about this recall
Why was it recalled?
Potential for unintentional movement of the support surface of the bed from tilted position to horizontal position or any position in between.
Which lots are affected?
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
Where was it sold?
US distribution to Texas.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other Other Medical Devices recalls
All 13,778| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Citric Complete Dry Citric Acid Concentrate recalled | Nipro Renal Soultions USA | Other | Nationwide |
| Device | CLASS I | Kit: Epidural/Pain TQC 20/Cs recalled by Medical Action Industries | Medical Action Industries Inc. 306 | Sterility | 6 states |
| Device | CLASS II | Halyard IV Start Kit Non-Sterile recalled by Avid Medical | Avid Medical | Sterility | Nationwide |
| Device | CLASS I | Kit: Single Shot Epidural 20/Cs recalled by Medical Action Industries | Medical Action Industries Inc. 306 | Sterility | 6 states |
| Device | CLASS II | AMS Convenience Kit: Dsaek Pack - RX recalled | Windstone Medical Packaging | Device Malfunction | Nationwide |