{
  "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": "Broomfield",
      "address_1": "310 Interlocken Pkwy",
      "reason_for_recall": "Zimmer Bioment Spine, Inc. announces a voluntary field action for the Zyston¿ Transform Instrument Case and Zyston¿ Transform Implant Kit because the locking mechanism on the implant is not functioning as intended.",
      "address_2": "Suite 120",
      "product_quantity": "5",
      "code_info": "Lot Numbers: 2016244391; 2016244394; 2016244395; 2016244396; 2016244397; 2016244424; 2016244426; 2016244427; 2016244428; 2016244430.",
      "center_classification_date": "20160811",
      "distribution_pattern": "Nationwide to PA, TX, TN, NV, VA, WV, and KY. No Canadian, other foreign, VA/gov/military consignees.",
      "state": "CO",
      "product_description": "Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled sterile.",
      "report_date": "20160817",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet Spine, Inc",
      "recall_number": "Z-2398-2016",
      "initial_firm_notification": "Other",
      "product_type": "Devices",
      "event_id": "74687",
      "termination_date": "20170315",
      "more_code_info": "",
      "recall_initiation_date": "20160630",
      "postal_code": "80021-3479",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}