{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Foothill Ranch",
      "address_1": "90 Icon",
      "reason_for_recall": "Incorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter.",
      "address_2": "",
      "product_quantity": "4,436",
      "code_info": "ORG 9100A serial numbers: 00001 to 01413  ORG 9110A serial numbers: 00001 to 02706   ORG 9700A serial numbers: 00001 to 00894",
      "center_classification_date": "20210302",
      "distribution_pattern": "US - AL, AZ, AR, CA, CO, CT, DE, DC, FL, GA, HI, ID, IL, IN, IA, KS,KY, LA, ME, MA, MD, MI, MS, MS, MO, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA WI, WV and WY.",
      "state": "CA",
      "product_description": "WMTS Telemetry Receiver, Multiple Patient Receiver,  Model Number/ UDI:  ORG 9100A/ 00841983102554  ORG 9110A/ 00841983102561  ORG 9700A/No UDI",
      "report_date": "20210310",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Nihon Kohden America Inc",
      "recall_number": "Z-1162-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "87264",
      "more_code_info": "",
      "recall_initiation_date": "20210108",
      "postal_code": "92610-3000",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}