Civco Medical Instruments Co. Inc. recalls eTRAX Needle Sensor
- Recalling company
- Civco Medical Instruments Co. Inc.
- Product
- eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 2, 2026
- Reported
- Apr 8, 2026
- Distribution
- US States: OH, PA, WA. China.
- Status
- Ongoing
- Quantity
- 10 units
- Lot / codes
- UDI-DI: 00841436111096; Lot Number: A276636, A282454
- Company location
- Kalona, IA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1737-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1737-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.