Reported Dec 29, 2021 · Terminated
VirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX
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, 10 17 GA VirtuTRAX
- Lot codes and dates
- Part Number 610-1059
- UDI 00841436101882 Lot Numbers
A108295A111466A111759A112392A113288A113874A116720A118295A118557A119369A120039A120344A120567A120641A120807A121367A121506A121516A121866A122103A123138A124555A125980A127569A127842A129198A129948A129949A129950A130252A131213A131428A132258A132471A133741A133742A133823A134199A134203A135587A135846A136274A136787A137788A138199A138307A138805A139478A140029A140660A142719A143236A144157A144317A144992A145774
- Amount recalled
- 599 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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