CLASS II Device recall · Reported 20 May 2020 · FDA Enforcement Report
Quickie/Zippie powered wheelchair recalled by Sunrise Medical (US)
Sunrise Medical (US) is recalling Quickie/Zippie powered wheelchair, distributed in Montana. The recall was initiated on 13 Feb 2020 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-1947-2020
- FDA event ID
- 85431
- Recalling firm
- Sunrise Medical (US), Fresno, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 13 Feb 2020
- FDA classified
- 11 May 2020
- Reported
- 20 May 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Wheelchairs, Beds & Lifts
Timeline
| 13 Feb 2020 | Recall initiated by company | |
| 11 May 2020 | Classified by FDA | +88 days |
| 20 May 2020 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Due to programming errors in the Controller, an increase in the set motor parameters can be made by the end user beyond tested safe limits.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
Quickie/Zippie powered wheelchair. Q700M wheelchair. A battery operated powered wheelchair, which is controlled by Power Module RNET 120A Expandable (Item No.: 250ER10, Part No.: 123966).
Where it was distributed
Distributed to US Consignee in MT.
Questions about this recall
Is Quickie/Zippie powered wheelchair recalled?
Yes. Sunrise Medical (US) recalled Quickie/Zippie powered wheelchair on 13 Feb 2020. The recall is Class II and its status is Terminated. Recall number Z-1947-2020.
Why was it recalled?
Due to programming errors in the Controller, an increase in the set motor parameters can be made by the end user beyond tested safe limits.
Which lots are affected?
Q700M wheelchair S/N Q7MP-083941. UDI:(01)05022408059799. Power Module RNET 120A Expandable (Item No.: 250ER10, Part No.: 123966). Controller label: D50903.15 CR19100531.
Where was it sold?
Distributed to US Consignee in MT.
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 21 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 (US)
All 10| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Zippie Voyage, early intervention stroller recalled | Sunrise Medical (US) | Other | Nationwide |
| Device | CLASS II | Zippie Voyage, early intervention stroller recalled | Sunrise Medical (US) | Other | Nationwide |
| Device | CLASS II | Quickie Q7 wheelchair recalled by Sunrise Medical (US) | Sunrise Medical (US) | Device Malfunction | CA |
| Device | CLASS II | Quickie IRIS Wheelchair recalled by Sunrise Medical (US) | Sunrise Medical (US) | Device Malfunction | Nationwide |
| Device | CLASS II | Zippie IRIS Wheelchair recalled by Sunrise Medical (US) | Sunrise Medical (US) | Device Malfunction | Nationwide |
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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 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 |