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Crédits
Devices
Device Recall IVC
Modèle / numéro de série
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.
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
involved products were distributed to approximately 1100 dealers in the United Stated and to 54 Canadian dealer accounts.
Description du dispositif
Invacare IVC Home Care Bed (Foot Section with new head actuator from Linak.
Manufacturer
Invacare Corporation
1 Event
Rappel de Device Recall IVC
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Fabricant
Invacare Corporation
Adresse du fabricant
Invacare Corporation, One Invacare Way, Elyria OH 44036
Source
USFDA
Language
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