Product Safety Recalls

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Civco Medical Instruments Co. Inc. Recall 88906

Description: VirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX

Civco Medical Instruments Co. Inc. Recall 88906 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0398-2022
Event ID88906
Event DescriptionVirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX
Product TypeDevices
DistributionWorldwide distribution - US Nationwide and the countries of Belgium, Canada, China (Mainland), China (Taiwan), Denmark, France, Germany, Italy, Japan, Netherlands, Singapore, South Korea, Spain, Thailand.
Quantity599 boxes (5 units/box)
Recall ReasonThere is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
Device Classification20211229
Device Code InfoPart Number 610-1059; UDI 00841436101882 Lot Numbers: A108295, A111466, A111759, A112392, A113288, A113874, A116720, A118295, A118557, A119369, A120039, A120344, A120567, A120641, A120807, A121367, A121506, A121516, A121866, A122103, A123138, A124555, A125980, A127569, A127842, A129198, A129948, A129949, A129950, A130252, A131213, A131428, A132258, A132471, A133741, A133742, A133823, A134199, A134203, A135587, A135846, A136274, A136787, A137788, A138199, A138307, A138805, A139478, A140029, A140660, A142719, A143236, A144157, A144317, A144992, A145774
Center Classification Date20211220
Recall Initiation Date20211008
Recalling FirmCivco Medical Instruments Co. Inc.
Initial Notification E-Mail
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