{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74867",
      "recalling_firm": "Integra LifeSciences Corp. d.b.a. Integra Pain Management",
      "address_1": "3498 W 2400 S Ste 1050",
      "address_2": "N/A",
      "postal_code": "84119-1135",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : OH and CA.  No foreign, Govt/VA/military consignee.",
      "recall_number": "Z-2684-2016",
      "product_description": "INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile.",
      "product_quantity": "200 packages (20 cases)",
      "reason_for_recall": "Integra LifeSciences is recalling Spinal Trays, Cat No. 3404875, because of the affected recalled Hospira 5% Lidocaine HCL that is a component of some lots of the  Spinal Trays.",
      "recall_initiation_date": "20160804",
      "center_classification_date": "20160829",
      "termination_date": "20161219",
      "report_date": "20160907",
      "code_info": "The affected lots of Integra¿ Spinal Trays were manufactured on 2/11/205 and on 7/11/2015.  Lots: W1503004; S1501531; S1505556;"
    }
  ]
}