{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Middleton",
      "address_1": "3150 Pleasant View Rd",
      "reason_for_recall": "Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may exhibit excessive background noise that may mask the user\u0019s ability to clearly hear heart rate and/or blood flow.",
      "address_2": "",
      "product_quantity": "2,335 units total",
      "code_info": "Serial numbers: CHR0140  CHR0141  CHR0142  CHR0143  CHR0144  CHR0145  CHR0146  CHR0147  CHR0148  CHR0149  CHR0150  CHR0151  CHR0152  CHR0153  CHR0154  CHR0155  CHR0156  CHR0157  CHR0158  CHR0159  CHR0160, and   CHR0161.",
      "center_classification_date": "20170713",
      "distribution_pattern": "Worldwide Distribution -- US, to the following states: AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH , OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, and WV and, to the countries of Australia, Canada, Chile, Columbia, Germany, India, Japan, Jordan, Kuwait, Netherlands, Papua Guinea, Philippines, Qatar, Saudi Arabia, Singapore, Sweden, Switzerland, Thailand, and United Kingdom.",
      "state": "WI",
      "product_description": "Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe, Model #: X1L008, Catalog Code: NW20.    Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.",
      "report_date": "20170719",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Natus Neurology Inc",
      "recall_number": "Z-2727-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77569",
      "termination_date": "20200722",
      "more_code_info": "",
      "recall_initiation_date": "20170609",
      "postal_code": "53562-4800",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}