CLASS II Device recall · Reported 11 Jan 2017 · FDA Enforcement Report
TRU-Balance 3 Power Positioning Systems recalled
Pride Mobility Products is recalling TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen . Mobility Medical, distributed nationwide in the US. The recall was initiated on 1 Dec 2016 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-0942-2017
- FDA event ID
- 75881
- Recalling firm
- Pride Mobility Products, Exeter, PA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 1 Dec 2016
- FDA classified
- 3 Jan 2017
- Reported
- 11 Jan 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Wheelchairs, Beds & Lifts
Timeline
| 1 Dec 2016 | Recall initiated by company | |
| 3 Jan 2017 | Classified by FDA | +33 days |
| 11 Jan 2017 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The interface between the TB3 back and tilt base can separate when tilted beyond the specified angle.
Product as listed by the FDA
TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1). Mobility Medical Device
Where it was distributed
Nationwide Distribution
Questions about this recall
Why was it recalled?
The interface between the TB3 back and tilt base can separate when tilted beyond the specified angle.
Which lots are affected?
Numerous serial numbers affected (12,343 units)
Where was it sold?
Nationwide Distribution
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.
More recalls from Pride Mobility Products
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| Device | CLASS II | Quantum Rehab Quantum 4Front 2HD recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
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Other Wheelchairs, Beds & Lifts recalls
All 172| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Quantum Rehab Quantum 4Front 2HD recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge 2.0 (ilevel) recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |