{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91193",
      "recalling_firm": "Natus Medical Incorporated",
      "address_1": "5955 Pacific Center Blvd",
      "address_2": "",
      "postal_code": "92121-4309",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the states of AK, CA, CT, DC, FL, GA, IA, ID, IL, KS , MD, MI, MT, ND, NE, NJ, NV, NY, OH, OR, TX, and WA.",
      "recall_number": "Z-0735-2023",
      "product_description": "The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set that is used to create an intracranial burr-hole typically required for procedures such as ventriculostomy or intracranial pressure (ICP) monitoring. The various components of the kit are comprised to make it convenient for the practitioner to have all that they need in one place for fast and efficient intracranial access. cerebral spinal fluid (CSF).",
      "product_quantity": "249 kits",
      "reason_for_recall": "Due to Cranial Access Kits containing recalled sterile surgical drapes.  The sterile surgical drapes are being recalled due to the liner on the adhesive component is difficult to remove without damaging the product and may render the product unusable.",
      "recall_initiation_date": "20221118",
      "center_classification_date": "20221220",
      "report_date": "20221228",
      "code_info": "Part Number: HITH1 UDI-DI Code: 382830048590 Lot Number: 22GDB675  Part Number: HITHNDRZR UDI-DI Code: 382830048620 Lot Number: 22HDA557  Part Number: HITHLT UDI-DI Code: 382830048637 Lot Number: 22IDB724",
      "more_code_info": ""
    }
  ]
}