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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Civco Medical Instruments Co. Inc.: There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.

Agency Publication Date: December 20, 2021
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Affected Products

Product: VirtuTRAX Instrument Navigator, 14 Ga VirtuTRAX

Part Number 610-1153; UDI 00841436102285; Lot Numbers: A122182, A131167, A131689, A131691, A141823

Lot Numbers:
Numbers
Product: VirtuTRAX Instrument Navigator, Sensor with 10 17 GA VirtutTRAX

Part Number 610-1080; UDI 00841436101936; Lot Numbers: A109102, A109175, A121363, A129087, A129088, A131042, A133436, A134220, A138099, A139369, A140674, A141818

Lot Numbers:
Numbers
Product: VirtuTRAX Instrument Navigator, Sensor with 14 Ga VirtutTRAX

Part Number 5350925; UDI 00841436100892; Lot Numbers: A117795, A119539, A121993, A129844, A131074, A131075, A131690, A142178

Lot Numbers:
Numbers
Product: VirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX

Part 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

Lot Numbers:
Numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 88906
Status: Resolved
Manufacturer: Civco Medical Instruments Co. Inc.
Manufactured In: United States
Units Affected: 4 products (52 boxes (5 units/box); 9 boxes (5 units/box); 18 boxes (5 units/box); 599 boxes (5 units/box))

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.