{
  "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": [
    {
      "country": "United States",
      "city": "Scottsdale",
      "address_1": "16597 N 92nd St Ste 101",
      "reason_for_recall": "Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.",
      "address_2": "",
      "product_quantity": "976 units",
      "code_info": "Item Number (Lot Number): CM-2409 (40731-2, 40743-5, 41049-1, 41237-2, 41536-2, 41737-2, 42219-2), CM-2410 (40731-3, 40743-6, 41049-2, 41237-3, 41536-3, 41737-3, 42219-3).",
      "center_classification_date": "20180710",
      "distribution_pattern": "US nationwide distribution.",
      "state": "AZ",
      "product_description": "AperFix AM Femoral Implant, Model numbers CM-2409 (9mm x 24 mm) and CM-2410 (10 mm x 24 mm).  For orthopedic use in ligament reconstruction.",
      "report_date": "20180718",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cayenne Medical Inc.",
      "recall_number": "Z-2422-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80282",
      "termination_date": "20180914",
      "more_code_info": "",
      "recall_initiation_date": "20130711",
      "postal_code": "85260-1847",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}