Z-1510-06

Solara Spree GT manual wheelchair

Name: Z-1510-06 Solara Spree GT manual wheelchair
Creator: Invacare Corporation
Published: 2006-06-27
License: https://open.fda.gov/license/

Invacare GmbH / initiated 2006-06-27 / Terminated

FDA source

Invacare Corporation began a recall of Solara Spree GT manual wheelchair on 2006-06-27. The reason FDA records is "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...". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1510-06
Status: Terminated
Initiated: 2006-06-27
Posted: 2006-09-20
Terminated: 2007-10-11
Recalling firm: Invacare GmbH
Product: Solara Spree GT manual wheelchair.
Product code: IOR Wheelchair, Mechanical
Reason for recall: 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.
FDA root cause: Other
Action: The recalling firm notified their consignees in a letter dated 6/26/06.
Quantity in commerce: 6 wheelchairs
Distribution: Nationwide and Canada.
Product codes and lots: 06EE011382, 06FE000065, 06FE001632, 06FE001635, 06FE006693, 06FE007246

Product code IOR

K012370Class ISolara Jr. Manual WheelchairInvacare Corp. / cleared 2001-08-03

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)