{
  "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": "2026-04-22",
    "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": "67675",
      "recalling_firm": "Pega Medical Inc.",
      "address_1": "1111 Autoroute Chomedy",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide in the states of  Missouri, Texas, and the country of Germany.",
      "recall_number": "Z-1448-2014",
      "product_description": "Pega Medical Inc., Fassier-Duval IM Telescopic System, male component (solid shaft),  Part number: M040-SS-110; Used in Implant Catalogue number: FD-040(LS)-SS. orthopedic intramedullary rod.",
      "product_quantity": "Total of 5 units (2 units in the US and 3 units in Germany)",
      "reason_for_recall": "The Male Components in this lot are made of material with lower strength than manufacturing specifications.",
      "recall_initiation_date": "20140207",
      "center_classification_date": "20140410",
      "termination_date": "20140423",
      "report_date": "20140416",
      "code_info": "Lot #: 130424-15 (only laser marked on the Part Number: M040-SS-110);    Lot #: 121109-11 &130424-15 [Indicated on the label of the Catalogue Number: FD-040(L)-SS]."
    }
  ]
}