Recall archive / FDA device enforcement
eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149 — FDA record Z-1731-2026
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Mar 2, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149
- 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
- Recalling firm
- Civco Medical Instruments Co. Inc.
- Quantity
- 2 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1731-2026
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI-DI: 00841436111034; Lot Number: A228672 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US States: OH, PA, WA. China.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Apr 8, 2026
- Recall initiation date
- Mar 2, 2026
- Center classification date
- Apr 1, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.