FDA Medical Device Recalls (openFDA)
Sunrise Medical Inc: Quickie Groove Power Wheelchair with QC (non-expandable) electronics, Model number EIPW13.
- Recall number
- Z-1532-2008
- Recalling firm
- Sunrise Medical Inc
- Product
- Quickie Groove Power Wheelchair with QC (non-expandable) electronics, Model number EIPW13.
- Status
- Terminated
- Initiated
- 2008-01-11
- Posted
- 2008-08-23
- Terminated
- 2009-11-16
- Reason
- Product experiences a longer than expected stopping distance, which may cause injury to the user, objects, or the chair itself.
- Root cause
- Software design
- Action
- Initial phone contact began on January 11, 2008. Medical device correction letters were also sent to affected dealers.
- Quantity
- 141 units total
- Distribution
- Product was distributed to 126 retailers nationwide throughout the USA, as well as Canada and Australia.
- Lot, serial or model codes
- All wheelchairs with the QC Motor controller units with version 2.0 parameter or *.SUN file software.
- 510(k) numbers
- ["K060531"]
- PMA numbers
- not on file
- Product code
- ITI
- Firm FEI
- 2937137
- Firm city
- Fresno
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28