{
  "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": [
    {
      "status": "Terminated",
      "city": "Golden",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72686",
      "recalling_firm": "Bestmed, LLC",
      "address_1": "331 Corporate Cirle Unit E",
      "address_2": "N/A",
      "postal_code": "80401",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide Distribution and the country of Canada.",
      "recall_number": "Z-0412-2016",
      "product_description": "Digital Temple Thermometer labeled under: Bestmed, Good Neighbor (Amerisource Bergen), Kroger, Medline, Meijer, Premier Value, Safeway, Life Brand, Target, Top Care, Best Choice, Western Family. Device is packaged in plastic blister with cardboard insert, 2 AAA batteries installed, a Quick Start Guide, and an Instruction Manual booklet.    Product Usage:  Device is a handheld thermometer that employs a thermistor sensor intended for people to take a human body temperature at the temporal artery location, the area between the outer corner of the eye and the hairline directly over the temporal artery.",
      "product_quantity": "305,548",
      "reason_for_recall": "An incorrect calibration of the thermometer that causes the device to display inaccurate and frequently lower temperatures than the actual body temperature of the user.",
      "recall_initiation_date": "20151112",
      "center_classification_date": "20151216",
      "termination_date": "20161130",
      "report_date": "20151223",
      "code_info": "Model KD-2201. all lots produced during the 36th week of  year 2012 (09/03-07/2012) through and including the 37th week of year 2015 (09/07-13/2015). Lot No. \u001cS/N: 3612\u001d through \u001cS/N: 3715\""
    }
  ]
}