{
  "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": "83372",
      "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": "CA, DE, FL, IL, NC, NE, NY and TN",
      "recall_number": "Z-2278-2019",
      "product_description": "SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System",
      "product_quantity": "19",
      "reason_for_recall": "Handle could jam with the Driver due to the detachment of an internal Connector Ring.",
      "recall_initiation_date": "20190529",
      "center_classification_date": "20190814",
      "termination_date": "20210115",
      "report_date": "20190821",
      "code_info": "Lot # 150115-09, 160427-01 and A162-02"
    }
  ]
}