FDA recall record

Civco Medical Instruments Co eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number recall — FDA Z-1736-2026

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…

Class IIclassification
Z-1736-2026official record ID
Apr 8, 2026report date

Recall record at a glance

Official recordZ-1736-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCivco Medical Instruments Co. Inc.
Report dateApr 8, 2026
Recall initiation dateMar 2, 2026
Quantity5 units
LocationKalona, IA, United States

Official product description

eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157

Why the product was recalled

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.

Distribution information

US States: OH, PA, WA. China.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: not stated.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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