{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Hillsborough",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91338",
      "recalling_firm": "Trackx Technology Inc",
      "address_1": "437 Dimmocks Mill Rd Ste 28",
      "address_2": "",
      "postal_code": "27278-2379",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, FL, LA, NC, PA, VA, WA, WI.",
      "recall_number": "Z-1107-2023",
      "product_description": "TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile;  and TrackX Insight Base Modular Instrument Tracker, 6.5L, Model #605-3TX, Sterile.",
      "product_quantity": "464 devices",
      "reason_for_recall": "The device is breaking and falling off the Nuvasive T-Handle with Hudson Adapter on certain Nuvasive XLIF instruments during surgery when malleted.",
      "recall_initiation_date": "20221024",
      "center_classification_date": "20230209",
      "report_date": "20230215",
      "code_info": "Insight Base -5L - Lot #2206001, exp. 6/1/2025, UDI 00857088008431; Insight Base 6.5L - Lot #2202002,  exp. 2/1/20024, UDI 00857088008448.",
      "more_code_info": ""
    }
  ]
}