Civco recalls eTRAX Needle System Starter Kit 12G (Part 667-149) due to potential incorrect needle tip position display on Aurora Trackers. Affected units have UDI-DI 0084143:111034 and Lot A228672.
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 12G for Aurora Trackers because the needle sensor may show the wrong position on the user interface. This could lead to improper needle placement during medical procedures.
The needle sensor may incorrectly identify the needle tip position on the user interface. This could result in improper needle placement during medical procedures if the system is used without noticing the error.
Medical professionals using the eTRAX Needle System Starter Kit 12G with Aurora Trackers are most at risk. Affected units have specific part numbers and lot numbers.
Check for the part number 667-149 and lot number A228672 on the eTRAX Needle System Starter Kit 12G. The UDI-DI code 00841436111034 is also associated with this recall.
Verify the part number 667-149 and lot number A228672 on the eTRAX Needle System Starter Kit 12G.
The recall indicates a potential for incorrect needle tip position display, which could lead to improper needle placement during medical procedures. However, the remedy is not specified, so the risk level is low.
The recall record does not specify a remedy, so no action is required beyond checking product details for the part number and lot number.
Check for part number 667-149 and lot number A228672 on the eTRAX Needle System Starter Kit 12G. The UDI-DI code 00841436111034 is also associated with this recall.
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-1731-2026 — Civco Medical Instruments Civco Medical Instruments Hello, I own a Civco Medical Instruments that is covered by recall Z-1731-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
