{
  "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": "Laval",
      "state": "",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71560",
      "recalling_firm": "Pega Medical Inc.",
      "address_1": "1111 Autoroute Chomedy",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution to the states of : FL and TN.",
      "recall_number": "Z-1848-2015",
      "product_description": "Slipped Capital Femoral Epiphysis (SCFE) Drivers of the Free-Gliding SCFE Screw System with catalogue number SCF-MLD265 and SCF-MLD273.",
      "product_quantity": "4 units",
      "reason_for_recall": "SCFE Drivers of the Free-Gliding SCFE Screw System are recalled because the handle of the instruments may detach from the shaft if high torques are applied in counter-clockwise rotation.",
      "recall_initiation_date": "20150615",
      "center_classification_date": "20150626",
      "termination_date": "20151229",
      "report_date": "20150708",
      "code_info": "Part Number: SCF-MLD265, LOT#: 130703-01.  Part Number: SCF-MLD273, LOT#: 130703-02.",
      "more_code_info": ""
    }
  ]
}