{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74484",
      "recalling_firm": "Encore Medical, Lp",
      "address_1": "9800 Metric Blvd",
      "address_2": "N/A",
      "postal_code": "78758-5445",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CO, ID, TX",
      "recall_number": "Z-2242-2016",
      "product_description": "MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636",
      "product_quantity": "14 (7 sets)",
      "reason_for_recall": "Reported failure of the instrument.  The retaining ring component of a neck trial became disassembled from the body of the neck.",
      "recall_initiation_date": "20160621",
      "center_classification_date": "20160719",
      "termination_date": "20170110",
      "report_date": "20160727",
      "code_info": "Lot: 313R1000, 313R1900, 313R1901, 314R1000, 314R1900, 314R1901",
      "more_code_info": ""
    }
  ]
}