{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "64654",
      "product_res_number": "Z-0331-2008",
      "event_date_initiated": "2007-09-27",
      "event_date_posted": "2007-12-08",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-06-21",
      "res_event_number": "44963",
      "k_numbers": [
        "K051983",
        "K052491",
        "K060970"
      ],
      "product_description": "Axya Bone Anchor , 3.0 mm Titanium with Nylon Suture\nCatalog Number: CAT1226, Axya Medical, Inc., Beverly, MA 01915",
      "code_info": "Lot Numbers: 203213, 203233, 203335, 203465, 203720, 203736, 204367, 204413, 204695, and 204802",
      "firm_fei_number": "3000718467",
      "recalling_firm": "Axya Medical",
      "address_1": "100 Cummings Ctr Ste 444c 100 Cummings Ctr",
      "address_2": "Ste 444c",
      "city": "Beverly",
      "state": "MA",
      "postal_code": "01915-6132",
      "additional_info_contact": "SAME\n978-232-9997 Ext. 647",
      "reason_for_recall": "Sterility Compromised (Package Integrity): Sterility of the device may be compromised due to holes in the sterile packaging",
      "root_cause_description": "Package design/selection",
      "action": "Axya  Medical notified customers by letter, Urgent-Product Recall,  dated 9/25/07 , via UPS . Users are requested to return product and complete the reply form.",
      "product_quantity": "1,008 units",
      "distribution_pattern": "Nationwide",
      "openfda": {}
    }
  ]
}