FDA Recall Open, Classified

eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158

Recall: Z-1737-2026 · Initiated March 2, 2026

Recall

Recall Number
Z-1737-2026
Event Number
98513
Firm
Civco Medical Instruments Co. Inc.
FEI Number
1937223
Product Code
IYO
Status
Open, Classified
Root Cause
Software change control
Initiated
March 2, 2026
Posted
April 1, 2026
Address
102 1st St S, Kalona, IA, 52247-9589

Description

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.

Action

An URGENT: MEDICAL DEVICE RECALL notification letter dated 3/2/26 was sent to customers. Actions to be taken by the Customer/User: CIVCO requests that you check your inventory for any eTRAX Needle Sensor for Aurora Trackers and complete the supplied response letter for the appropriate action. Please contact your distribution partner to return any existing inventory, or report its destruction by completing the attached response form. Please complete the enclosed response form even if you do not have any eTRAX Needle Sensor for Aurora Trackers remaining in your inventory to assist in our reconciliation process. Response forms can also be sent via email to [email protected]. For questions, contact CIVCO at # 800-445-6741, or 319-248-6757. Type of Action by the Company: This notice is being communicated to all customers who have purchased an eTRAX Needle Sensor for Aurora Trackers from affected lots. CIVCO requests you provide this notification to the appropriate personnel within your facility. If the affected product was distributed outside of your organization, please notify those locations down to the medical facility level.

Distribution

US States: OH, PA, WA. China.

Quantity

10 units