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Devices
Device Recall IVC
Model / Serial
Foot section model numbers and serial number ranges: Model # Beginning S/N Ending S/N 5490IVC 03D891256 03E035155 5890IVC 03D889942 03E002241 5491IVC 03E969254 03E433379 5891IVC 03E970154 03E971163 Bed Models that include the recalled food sections: 5310IVC, 5311IVC, 5410IVC, 5411IVC Bed package model numbers which include the affected Beds and foot sections: BED-21VC, BED-4IVC, BED-9IVC, BED-10IVC, BED-19IVC, BED-21IVC, BED-22IVC, BED-23IVC, BED-24IVC, BED-25IVC, BED-26IVC, BED-27IVC, BED-28IVC, BED-29IVC, BED-32IVC, BED-33IVC, BED-34IVC, BED-35IVC, BED-36IVC, BED-37IVC, CBED-2IVC, CBED-4IVC, CBED-4BIVC, CBED-11IVC, CBED-11BIVC, CBED-12IVC, CBED-12BIVC, CBED-19IVC, CBED-22IVC, CBED-23IVC, CBED-26IVC, CBED-28IVC.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
involved products were distributed to approximately 1100 dealers in the United Stated and to 54 Canadian dealer accounts.
Product Description
Invacare IVC Home Care Bed (Foot Section with new head actuator from Linak.
Manufacturer
Invacare Corporation
1 Event
Recall of Device Recall IVC
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Manufacturer
Invacare Corporation
Manufacturer Address
Invacare Corporation, One Invacare Way, Elyria OH 44036
Source
USFDA
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