Invacare Corporation Solara 2G manual wheelchair. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Solara 2G manual wheelchair.
Brand
Invacare Corporation
Lot Codes / Batch Numbers
06EE008858, 06EE010422, 06EE010432, 06EE010434, 06EE010442, 06EE010453, 06EE010454, 06EE010745, 06EE010747, 06EE010749, 06EE010758, 06EE010799, 06EE010804, 06EE010810, 06EE011357, 06EE011378, 06EE011379, 06FE000048, 06FE000050, 06FE000054, 06FE000055, 06FE000057, 06FE000985, 06FE001000, 06FE001012, 06FE001604, 06FE001612, 06FE001625, 06FE006654, 06FE006661, 06FE007243, 06FE008820, 06FE008829, 06FE008832, 06FE009212, 06FE010083.
Products Sold
06EE008858, 06EE010422, 06EE010432, 06EE010434, 06EE010442, 06EE010453, 06EE010454, 06EE010745, 06EE010747, 06EE010749, 06EE010758, 06EE010799, 06EE010804, 06EE010810, 06EE011357, 06EE011378, 06EE011379, 06FE000048, 06FE000050, 06FE000054, 06FE000055, 06FE000057, 06FE000985, 06FE001000, 06FE001012, 06FE001604, 06FE001612, 06FE001625, 06FE006654, 06FE006661, 06FE007243, 06FE008820, 06FE008829, 06FE008832, 06FE009212, 06FE010083.
Invacare Corporation is recalling Solara 2G manual wheelchair. due to The wheelchairs with the Travel Ready Option (TRRO) may contain incorrectly finished oval tie down brackets. The inner edge of the bracket may cause. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
The recalling firm notified their consignees in a letter dated 6/26/06.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026