CLASS II Device recall · Reported 8 Aug 2012 · FDA Enforcement Report
Padded Swing Away Arm Rest with Receiver recalled
Sunrise Medical is recalling Padded Swing Away Arm Rest with Receiver, distributed nationwide in the US. The recall was initiated on 26 Jun 2012 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-2113-2012
- FDA event ID
- 62493
- Recalling firm
- Sunrise Medical, Fresno, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 26 Jun 2012
- FDA classified
- 31 Jul 2012
- Reported
- 8 Aug 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Wheelchairs, Beds & Lifts
Timeline
| 26 Jun 2012 | Recall initiated by company | |
| 31 Jul 2012 | Classified by FDA | +35 days |
| 8 Aug 2012 | 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
Reports of injury when the Padded Swing Away Armrest is used for full body weight. Owner's manual states that armrest is only designed for resting of forearm.
Product as listed by the FDA
Padded Swing Away Arm Rest with Receiver; Uses on wheelchair models: Quickie Q7 (EIR4), GT (EIR3), GTi (EIT4) and Zippie Zone (EIRZ1). Product Usage: To empower physically challenged persons by providing a means of mobility. This includes temporary and permanent conditions.
Where it was distributed
Worldwide Distribution - US (nationwide) and the countries of Argentina, Brazil, Columbia, Costa Rica, Mexico, Panama, Uruguay and Venezuela.
Questions about this recall
Why was it recalled?
Reports of injury when the Padded Swing Away Armrest is used for full body weight. Owner's manual states that armrest is only designed for resting of forearm.
Which lots are affected?
Receiver Product number 109207.
Where was it sold?
Worldwide Distribution - US (nationwide) and the countries of Argentina, Brazil, Columbia, Costa Rica, Mexico, Panama, Uruguay and Venezuela.
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 Sunrise Medical
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|---|---|---|---|---|---|
| Device | CLASS II | Zippie Voyage, early intervention stroller recalled | Sunrise Medical | Other | Nationwide |
| Device | CLASS II | Zippie Voyage, early intervention stroller recalled | Sunrise Medical | Other | Nationwide |
| Device | CLASS II | Quickie/Zippie powered wheelchair recalled by Sunrise Medical (US) | Sunrise Medical | Device Malfunction | MT |
| Device | CLASS II | Quickie Q7 wheelchair recalled by Sunrise Medical (US) | Sunrise Medical | Device Malfunction | CA |
| Device | CLASS II | Quickie IRIS Wheelchair recalled by Sunrise Medical (US) | Sunrise Medical | Device Malfunction | Nationwide |
Other Wheelchairs, Beds & Lifts recalls
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|---|---|---|---|---|---|
| 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 |