Reported Dec 29, 2021 · Terminated

VirtuTRAX Instrument Navigator, Sensor with 14 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 14 Ga VirtutTRAX
Lot codes and dates
    • Part Number 5350925
    • UDI 00841436100892
  • Lot Numbers
    • A117795
    • A119539
    • A121993
    • A129844
    • A131074
    • A131075
    • A131690
    • A142178
Amount recalled
52 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?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 6:58 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.