Reported Apr 8, 2026 · Ongoing
eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152
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?
- eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152
- Lot codes and dates
- UDI-DI00841436111065
- Lot Number
A233347A228677A268116A268238A272513A279457A280388A281840
- Amount recalled
- 20 units
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
Why it was recalled
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
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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