{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Seongnam",
      "state": "N/A",
      "country": "Korea (the Republic of)",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98312",
      "recalling_firm": "Aju Pharm Co., Ltd.",
      "address_1": "Room 201, Room 207, Bl A",
      "address_2": "Bundangtekeunopakeu; 697 Pangyo-Ro; Bundang",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA & PR.",
      "recall_number": "Z-1171-2026",
      "product_description": "Genesis Push-In Suture Anchor",
      "product_quantity": "200 units",
      "reason_for_recall": "Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.",
      "recall_initiation_date": "20251217",
      "center_classification_date": "20260126",
      "report_date": "20260204",
      "code_info": "Model No.  10S30002; All UDI Codes; All Lots."
    }
  ]
}