FDAFDA · Food and drugs·Recall number Z-1734-2026
eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152
Published April 8, 2026 · Recall initiated: March 2, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated
Recall details
- Manufacturer
- Civco Medical Instruments Co. Inc.
- Distributor
- US States: OH, PA, WA. China.
- Lot
- UDI-DI: 00841436111065; Lot Number: A233347, A228677, A268116, A268238, A272513, A279457, A280388 , A281840
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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