Reported Dec 29, 2021 · Terminated

VirtuTRAX Instrument Navigator, Sensor with 10 17 GA VirtutTRAX

Civco Medical Instruments Co. Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Civco Medical Instruments Co. Inc. · 102 1st St S · Kalona, IA · 52247-9589

Is this the product you have?

  • VirtuTRAX Instrument Navigator, Sensor with 10 17 GA VirtutTRAX
Lot codes and dates
    • Part Number 610-1080
    • UDI 00841436101936
  • Lot Numbers
    • A109102
    • A109175
    • A121363
    • A129087
    • A129088
    • A131042
    • A133436
    • A134220
    • A138099
    • A139369
    • A140674
    • A141818
Amount recalled
18 boxes (5 units/box)

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Sep 30, 2024 · Data as of Sep 19, 4:53 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.