{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "2850 Frontier Dr",
      "reason_for_recall": "The 7mm diameter uniaxial pedicle screws have been color anodized with the same color utilized on 5 mm diameter screws.",
      "address_2": "",
      "product_quantity": "24 units",
      "code_info": "Model number: 00-1300-0740, Lot number: M82791-1",
      "center_classification_date": "20180213",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "IN",
      "product_description": "Response 5.5/6.0 Spine System   7.0mm x 40mm  Pedicle Screw    Product Usage:  Posterior non-cervical pedicle screw fixation",
      "report_date": "20180221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "OrthoPediatrics Corp",
      "recall_number": "Z-0597-2018",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "79067",
      "termination_date": "20190508",
      "more_code_info": "",
      "recall_initiation_date": "20170803",
      "postal_code": "46582-7001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}