FDA Medical Device Recalls (openFDA)
Sunrise Medical Inc: Sunrise Medical Quickie Groove Power Wheelchair with Transit option The product is a powered wheelchair for human use.
- Recall number
- Z-2339-2008
- Recalling firm
- Sunrise Medical Inc
- Product
- Sunrise Medical Quickie Groove Power Wheelchair with Transit option The product is a powered wheelchair for human use.
- Status
- Terminated
- Initiated
- 2006-11-13
- Posted
- 2008-09-23
- Terminated
- 2009-12-22
- Reason
- Rear bolts holding the frame in place may shear and the front bolts may potentially come off the posts, resulting in partial or full seat detachment in a sudden stop or crash.
- Root cause
- Device Design
- Action
- Initial phone contacts began on November 13, 2006. Letters were also mailed. The letter informed the customer of the problem and provided interim steps to take, until an transit upgrade kit is installed. Response cards will be tracked to measure response rate and assure receipt of notice. Contact Sunrise Medical at 1-800-456-8168 for assistance.
- Quantity
- 36 units
- Distribution
- Worldwide: US, Canada, New Zealand and Australia.
- Lot, serial or model codes
- Multiple serial numbers, starting with GRV-100: 182, 181, 178, 176, 166, 161, 160, 151, 150, 115, 110, 109, 106, 100, 099, 098, 094, 082, 081, 079, 076, 073, 064, 058, 056, 054, 053, 050, 044, 043, 041, 040, 035, 033, 021 and 013
- 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