Civco Medical Instruments Co. Inc.: Medical Device Recall in 2021 - (Recall #: Z-0398-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

VirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX

Product Classification:

Class II

Date Initiated: October 8, 2021

Date Posted: December 29, 2021

Recall Number: Z-0398-2022

Event ID: 88906

Reason for Recall:

There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.

Status: Terminated

Product Quantity: 599 boxes (5 units/box)

Code Information:

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

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Belgium, Canada, China (Mainland), China (Taiwan), Denmark, France, Germany, Italy, Japan, Netherlands, Singapore, South Korea, Spain, Thailand.

Voluntary or Mandated:

Voluntary: Firm initiated