CLASS II Device recall · Reported 4 Feb 2015 · FDA Enforcement Report

Quickie Q7 Adult Rigid Wheelchair recalled by Sunrise Medical (US)

Sunrise Medical is recalling Quickie Q7 Adult Rigid Wheelchair, distributed nationwide in the US. The recall was initiated on 19 Dec 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSerial numbers: R4-025066, R4-025051, R4-025010, R4-024771, R4-024738, R4-024649.

Quantity recalled6

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-1020-2015
FDA event ID: 70141
Recalling firm: Sunrise Medical, Fresno, CA
Classification: Class II
Status: Terminated
Recall initiated: 19 Dec 2014
FDA classified: 27 Jan 2015
Reported: 4 Feb 2015
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Wheelchairs, Beds & Lifts

Timeline

19 Dec 2014	Recall initiated by company
27 Jan 2015	Classified by FDA	+39 days
4 Feb 2015	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

There is the potential for the height adjustable handle to dislodge due to failing locking mechanisms on specific identified chairs.

Product as listed by the FDA

Quickie Q7 Adult Rigid Wheelchair Model EIR4.

Where it was distributed

Nationwide Distribution in the states of CO and ME.

Nationwide Colorado Maine

Questions about this recall

Why was it recalled?

There is the potential for the height adjustable handle to dislodge due to failing locking mechanisms on specific identified chairs.

Which lots are affected?

Serial numbers: R4-025066, R4-025051, R4-025010, R4-024771, R4-024738, R4-024649.

Where was it sold?

Nationwide Distribution in the states of CO and ME.

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 products in this recall event

1 other product · FDA event 70141

Reported	Class	Recall	Company	Reason	Where
4 Feb 2015	CLASS II	Zippie Zone Pediatric Rigid Wheelchair recalled by Sunrise Medical (US)	Sunrise Medical	Other	Nationwide

More recalls from Sunrise Medical

All 10

Reported	Class	Recall	Company	Reason	Where
4 Aug 2021Device	CLASS II	Zippie Voyage, early intervention stroller recalled	Sunrise Medical	Other	Nationwide
4 Aug 2021Device	CLASS II	Zippie Voyage, early intervention stroller recalled	Sunrise Medical	Other	Nationwide
20 May 2020Device	CLASS II	Quickie/Zippie powered wheelchair recalled by Sunrise Medical (US)	Sunrise Medical	Device Malfunction	MT
3 Aug 2016Device	CLASS II	Quickie Q7 wheelchair recalled by Sunrise Medical (US)	Sunrise Medical	Device Malfunction	CA
2 Sep 2015Device	CLASS II	Quickie IRIS Wheelchair recalled by Sunrise Medical (US)	Sunrise Medical	Device Malfunction	Nationwide

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