Civco recalls eTRAX 14G needle sensors for Aurora Trackers due to potential incorrect needle 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 eTR:AX 14G needle sensors for Aurora Trackers because they may show the wrong needle position on the device. This could lead to inaccurate medical measurements if used for tracking during procedures.
The sensor may incorrectly display the needle's position on the user interface due to an error in inspection and programming. This could cause inaccurate tracking of the needle during medical procedures, potentially leading to incorrect measurements.
Users of Aurora Trackers with the eTRAX 14G needle sensor (part number 667-157) are affected. Medical professionals using these sensors for surgical tracking are most at risk.
Check for the part number 667-157 on the eTRAX 14G needle sensor. Affected units also have UDI-DI: 00841436111089 and lot number A276633.
Verify the part number 667-157 on the eTRAX 14G needle sensor to confirm if it's affected.
No, this recall specifically affects eTRAX 14G needle sensors with part number 667-157.
The recall record does not specify a remedy, so check with Civco Medical Instruments for guidance.
Look for part number 667-157, UDI-DI: 00841436111089, and lot number A276633 on the sensor.
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-1736-2026 — Civco Medical Instruments Civco Medical Instruments Hello, I own a Civco Medical Instruments that is covered by recall Z-1736-2026 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.
