Trackx Technology Inc: Device Recall

Recall #Z-0260-2025 · 09/03/2024

Class III: Low Risk

Recall Details

Recall Number
Z-0260-2025
Classification
Class III
Product Type
Device
Recalling Firm
Trackx Technology Inc
Status
Ongoing
Date Initiated
09/03/2024
Location
Hillsborough, NC, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
82

Reason for Recall

The patient label stickers may have the wrong expiration date recorded. The contract manufacturer entered the manufacturing date (2024-04-01) as the expiration date. The actual expiration date of the product is 2027-04-01. This is reflected on the carton label and sterile pouch label correctly.

Product Description

Product Name: Insight Base Flex - 8, Ref 608-3TX; The device consists of a sterile Snap that includes reflective features that facilitate imaging of the (attached) instrument using instrument tracking technology when used with a compatible tracking system. Each TrackX¿ Snap has a unique set of 2 or more reflective markers. By having unique configurations of reflective markers, it is possible to identify which TrackX Snap is in the field of view of the camera(s). As such, it is also possible to have multiple TrackX Snaps in the field at once and to have different TrackX Snaps for different surgical instruments. The device is considered to be a sterile accessory.

Distribution Pattern

NC, VA, FL, PA, NY

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.