FDA Device recall Z-0942-2017
TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1)
- FDA Device
- Class II
- terminated
- Published 2017-01-11
On 2017-01-11 the FDA classified a Class II recall of TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1) by Pride Mobility Products, citing the interface between the TB3 back and tilt base can separate when tilted beyond the specified angle.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0942-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-12-01 |
| Published | 2017-01-11 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Pride Mobility Products |
| Distribution | US |
Product
TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1). Mobility Medical Device
Reason
The interface between the TB3 back and tilt base can separate when tilted beyond the specified angle.
Identifiers
| code_info | Numerous serial numbers affected (12,343 units) |
|---|
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-0942-2017%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.