Devices

Device Recall Solara 2G manual wheelchair.

Model / Serial
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.
Product Classification
Physical Medicine Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide and Canada.
Product Description
Solara 2G manual wheelchair.
Manufacturer
Invacare Corporation
1 Event
- Recall of Device Recall Solara 2G manual wheelchair.

Manufacturer

Invacare Corporation

Manufacturer Address
Invacare Corporation, 1 Invacare Way, PO Box 4028, Elyria OH 44035
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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