{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86027",
      "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": "E-Mail",
      "distribution_pattern": "US Nationwide distribution including in the states of Al, CA, FL, GA, KY, MI, MO, NC, NY, OH, TX.",
      "recall_number": "Z-2742-2020",
      "product_description": "Orthopedics 6.0MM ROD, COCR, SINGLE HEX, 500MM LENGTH-The RESPONSE\" 5.5/6.0 Spine System is intended for immobilization and  stabilization of the posterior, non-cervical spine in skeletally mature patients as an adjunct to fusion for the following indications: degenerative disc disease  Model Number: 00-1300-6053",
      "product_quantity": "73 units",
      "reason_for_recall": "Product may have incorrect laser etched alignment lines,  the non-conforming laser etch may have compromised strength, lead to unintended fracture of the device",
      "recall_initiation_date": "20200706",
      "center_classification_date": "20200730",
      "report_date": "20200805",
      "code_info": "Lot Number: 108332-A    UDI: (01)0084113212400(10)108332A"
    }
  ]
}