{
  "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": [
    {
      "country": "United States",
      "city": "Austin",
      "address_1": "9800 Metric Blvd",
      "reason_for_recall": "The retaining ring on the neck trials has a potential to fail interoperatively.",
      "address_2": "",
      "product_quantity": "28 (14 REF S200635 and 14 S200636)",
      "code_info": "All Revision C trials.  REF S-2000635:  313R1000, 313R1900, 313R1901; REF S-200636:  314R1000, 314R1900, 314R1901.",
      "center_classification_date": "20200410",
      "distribution_pattern": "Distribution was made to CA, CO, MD, MN, OH, TX, and WA.  There was no foreign/military/government distribution.",
      "state": "TX",
      "product_description": "djosurgical Linear Neck Trials with Spring Sides, Standard, nonsterile, REF S-200635; and djosurgical Linear Neck Trials with Spring Sides, Lateral, nonsterile, REF S-200636.  The firm name on the label is djosurgical, Austin, TX.",
      "report_date": "20200422",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Encore Medical, LP",
      "recall_number": "Z-1692-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "85211",
      "more_code_info": "",
      "recall_initiation_date": "20180710",
      "postal_code": "78758-5445",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}