{
  "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": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77270",
      "recalling_firm": "OrthoPediatrics Corp",
      "address_1": "2850 Frontier Dr",
      "address_2": "N/A",
      "postal_code": "46582-7001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide Distribution-US distribution to: MO, NY, KY, FL, NC and OH; and countries of:  AUSTRALIA, FRANCE and SPAIN.",
      "recall_number": "Z-2321-2017",
      "product_description": "Response BandLoc 5.5/6.0 Tensioner Instrument    The Tensioner Instrument (01-1102-1000) is utilized to allow the surgeon to apply a recommended tension to the band and hold it in place during spine manipulation and set screw tightening.",
      "product_quantity": "82",
      "reason_for_recall": "Over-tensioning of the band resulting in damage to the band  causing it to rupture",
      "recall_initiation_date": "20170424",
      "center_classification_date": "20170608",
      "termination_date": "20170918",
      "report_date": "20170614",
      "code_info": "All lots  Product Number: 01-1102-1000"
    }
  ]
}