{
  "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": "Terminated",
      "city": "Laval",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84017",
      "recalling_firm": "Pega Medical Inc.",
      "address_1": "1111 Chomedey (A-13) E",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide distribution to CA, FL, GA, HI, LA, MA, MO, NC, NY, OK.      International distribution to AUSTRALIA, CANADA, DENMARK, GERMANY, ISRAEL, MEXICO, ROMANIA, RUSSIA, UNITED ARAB EMIRATES, UNITED KINGDOM",
      "recall_number": "Z-0270-2020",
      "product_description": "SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm  Orthopedic surgical instrument component, for hip surgery",
      "product_quantity": "31 devices",
      "reason_for_recall": "There is a potential for the screws to have become loosened during ultrasonic cleaning of the knobs and the screws may come out.",
      "recall_initiation_date": "20191002",
      "center_classification_date": "20191101",
      "termination_date": "20201026",
      "report_date": "20191113",
      "code_info": "Catalogue Numbers: SCF-KNB265, SCF-KNB273, SCF-KNB365, SCF-KNB373;      Lot Numbers: 160428-03, 160428-04, A182-05, A182-15, 160603-05, 160603-06, A183-06"
    }
  ]
}