FDA Medical Device Recalls (openFDA)
Invacare Corporation: Solara Spree GT manual wheelchair.
- Recall number
- Z-1510-06
- Recalling firm
- Invacare Corporation
- Product
- Solara Spree GT manual wheelchair.
- Status
- Terminated
- Initiated
- 2006-06-27
- Posted
- 2006-09-20
- Terminated
- 2007-10-11
- Reason
- The wheelchairs with the Travel Ready Option (TRRO) may contain incorrectly finished oval tie down brackets. The inner edge of the bracket may cause the tie-down straps (used to tie down the chairs during transport) to fray or be cut.
- Root cause
- Other
- Action
- The recalling firm notified their consignees in a letter dated 6/26/06.
- Quantity
- 6 wheelchairs
- Distribution
- Nationwide and Canada.
- Lot, serial or model codes
- 06EE011382, 06FE000065, 06FE001632, 06FE001635, 06FE006693, 06FE007246
- 510(k) numbers
- ["K012370"]
- PMA numbers
- not on file
- Product code
- IOR
- Firm FEI
- 3002889431
- Firm city
- Elyria
- Firm state
- OH
- 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