Product Safety Recalls

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Civco Medical Instruments Co. Inc. Recall 88906

Description: VirtuTRAX Instrument Navigator, 14 Ga VirtuTRAX

Civco Medical Instruments Co. Inc. Recall 88906 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0396-2022
Event ID88906
Event DescriptionVirtuTRAX Instrument Navigator, 14 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.
Quantity9 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 610-1153; UDI 00841436102285; Lot Numbers: A122182, A131167, A131689, A131691, A141823
Center Classification Date20211220
Recall Initiation Date20211008
Recalling FirmCivco Medical Instruments Co. Inc.
Initial Notification E-Mail
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