{
  "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": "Powell",
      "address_1": "200 Debusk Ln",
      "reason_for_recall": "DeRoyal manufactured four lots of HNICU-32, Hydro-Temp(R) Neonatal Temperature Skin Sensor incorrectly. The pins contained in the probe were soldered incorrectly. When probe is connected to the proper port, this defect results in the inability to read or display temperatures on the infant warming system.",
      "address_2": "",
      "product_quantity": "16 cases of 50 units (800 eaches)",
      "code_info": "Lot Numbers:  39098746, 39655101, 39985370, 40067795",
      "center_classification_date": "20151130",
      "distribution_pattern": "Distributed in the states of VA, AL, FL, and CA.",
      "state": "TN",
      "product_description": "HYDRO-TEMP(R) Neonatal Temperature Skin Sensor, REF HNICU-32, 50 units per box, NON STERILE, Rx only.",
      "report_date": "20151209",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "DeRoyal Industries Inc",
      "recall_number": "Z-0345-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "72454",
      "termination_date": "20170701",
      "more_code_info": "",
      "recall_initiation_date": "20151014",
      "postal_code": "37849-4703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}