Civco recalls eTRAX Needle System Starter Kit 14G (Part 667-1:150) due to potential incorrect needle tip position display on Aurora Trackers. Affected units have specific part numbers and lot numbers.
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.
Civco is recalling its eTRAX Needle System Starter Kit 14G for Aurora Trackers because the needle sensor may show the wrong position on the user interface. This could lead to inaccurate needle placement during medical procedures.
The eTRAX needle sensor has an error in inspection and programming that causes the user interface to display the needle tip position incorrectly. This could result in inaccurate needle placement during medical procedures, potentially affecting treatment outcomes.
Medical professionals using the eTRAX Needle System Starter Kit 14G for Aurora Trackers are most at risk. The recall affects specific units with the part number 667-150 and lot number A228673.
Check for the part number 667-150 and lot number A228673 on the eTRAX Needle System Starter Kit 14G (for Aurora Trackers). This kit was sold with the UDI-DI: 00841436111041.
Verify the part number 667-150 and lot number A228673 on the eTRAX Needle System Starter Kit 14G for Aurora Trackers.
The recall is for a potential error in needle position display, which could affect accuracy during medical procedures. However, the risk is low and does not involve immediate danger.
Check for the part number 667-150 and lot number A228673 on the eTRAX Needle System Starter Kit 14G for Aurora Trackers. This kit was sold with the UDI-DI: 00841436111041.
The recall does not specify a remedy, so contact Civco Medical Instruments for further instructions.
We’ve drafted a message you can send Civco Medical Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-1732-2026 — Civco Medical Instruments Civco Medical Instruments Hello, I own a Civco Medical Instruments that is covered by recall Z-1732-2026 from Civco Medical Instruments. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
