Civco recalls eTRAX Needle System Starter Kit 16G for Aurora Trackers due to potential incorrect needle tip position display on user interface. 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 their eTRAX Needle System Starter Kit 16G for Aurora Trackers because the needle sensor may show the wrong position on the device. This could lead to inaccurate medical procedures if the needle is placed incorrectly.
The eTRAX needle sensor may incorrectly identify the needle tip position on the user interface. This could cause the needle to be placed at the wrong location during medical procedures, potentially leading to inaccurate treatment.
Users of the eTR:AX Needle System Starter Kit 16G for Aurora Trackers who purchased the affected units with specific part numbers and lot numbers. Medical professionals using this kit for procedures are most at risk.
Check for the part number 667-151 and lot numbers A228675, A228676, A233854, A268115, A268237, A272509, A277538, or A280341 on the product packaging or documentation.
Verify the part number and lot numbers on the product packaging or documentation to confirm if it is affected.
The part number for the affected eTRAX Needle System Starter Kit is 667-151.
Affected lot numbers are A228675, A228676, A233854, A268115, A268237, A272509, A277538, and A280341.
The recall record does not specify a remedy or fix for this issue.
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-1733-2026 — Civco Medical Instruments Civco Medical Instruments Hello, I own a Civco Medical Instruments that is covered by recall Z-1733-2026 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.
