Civco Medical Instruments Co. Inc. 2026-04-08 Health serious FDA
Health · FDA · Recall #FDA-Z-1738-2026
eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159 Recall
Issued April 8, 2026 · Civco Medical Instruments Co. Inc.
In April 2026, Civco Medical Instruments Co. Inc. recalled the eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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 you should do
- 1 Stop using eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Civco Medical Instruments Co. Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Civco Medical Instruments Co. Inc.
- Category
- Health
- Recall date
- April 8, 2026
- Units affected
- Not reported
- Sold at
- US States: OH, PA, WA. China.
- Recall number
- FDA-Z-1738-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Civco Medical Instruments Co. Inc. has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.