{
  "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": "2026-08-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99188",
      "recalling_firm": "Innovasis, Inc",
      "address_1": "614 E 3900 S",
      "address_2": "",
      "postal_code": "84107-1902",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of TX, CA.",
      "recall_number": "Z-2859-2026",
      "product_description": "Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System",
      "product_quantity": "5",
      "reason_for_recall": "Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque instrument with undersized condition which could prevent mating tip from engaging with the pedicle screw tulip and rod during tightening, which may lead to surgical delay, intervention/alternative methods to perform final tightening step.",
      "recall_initiation_date": "20260522",
      "center_classification_date": "20260803",
      "report_date": "20260812",
      "code_info": "LS-749: UDI-DI: M711BTA2020, M711LS7490, Serial Numbers: 002, 003, 007,  012, 014",
      "more_code_info": ""
    }
  ]
}