{
  "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": "Cincinnati",
      "address_1": "4900 Charlemar Dr Bldg A",
      "reason_for_recall": "An investigation of an adverse trend of complaints conducted by Integra LifeSciences identified various product performance issues which could impact the functionality of the firm's Mayfield Composite Series Base Units and  Mayfield Skull Clamps. In order to prevent additional complaint reports, the firm decided to recall and replace certain lot codes of the Base Units and Skull Clamps that were d",
      "address_2": "",
      "product_quantity": "5 base units were distributed",
      "code_info": "The recalle product is identified with the Lot Numbers: 097547 and 096546.",
      "center_classification_date": "20121219",
      "distribution_pattern": "Nationwide Distribution including the states of AL, AR, AZ, CA, CO, CT, FL, GA, IL, IN, KY, MA, MD, MI, MN, MO, NC, NE, NJ, NM, NY, OH, OK, OR, PA TN, TX, UT, VA, WA and WI.",
      "state": "OH",
      "product_description": "MAYFIELD Composite Series Base Unit,  Model A3101, a Swivel Adaptor (A3018) is an integral component of the Base Unit, Model A3101.    The MAYFIELD Base Unit (A3101) is an operating room table accessory intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp is necessary, positional freedom is required and where X-ray imaging modalities will be used. A Swivel Adaptor (A3018) is an integral component of the Base Unit A3101.",
      "report_date": "20121226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Integra LifeSciences Corporation",
      "recall_number": "Z-0558-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63776",
      "termination_date": "20140221",
      "more_code_info": "",
      "recall_initiation_date": "20121105",
      "postal_code": "45227-1402",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}