{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "43535",
      "product_res_number": "Z-0514-06",
      "event_date_initiated": "2005-12-13",
      "event_date_posted": "2006-02-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-05-07",
      "res_event_number": "34324",
      "product_code": "JTC",
      "k_numbers": [
        "K871945"
      ],
      "product_description": "Microlab AT, part numbers 135001, 135001OOC, 135002, 135003, 135005, 135006, 135006R, 135007, 135008, 135016, 135028, 135029, 936400, 936400BLU.  \n\nMicrolab AT+ and Microlab AT+2, part numbers 142000, 142001, 142001R, 142002, 142003, 142005, 142006, 142006R, 142007, 142008, 142009, 142015, 142017, 142035, 142036",
      "code_info": "All codes included.",
      "firm_fei_number": "2915796",
      "recalling_firm": "Hamilton Co",
      "address_1": "4970 Energy Way",
      "city": "Reno",
      "state": "NV",
      "postal_code": "89502-4123",
      "additional_info_contact": "Wayne McAuliffe\n775-858-3000",
      "reason_for_recall": "Heat sinking on power boards may not operate as intended and the board may cease to operate.",
      "root_cause_description": "Other",
      "action": "On 12/15/05, the firm initiated the recall and its notification was via letters explaining the reason for the recall and requesting the product be returned.",
      "product_quantity": "1071 units",
      "distribution_pattern": "Product was released for distribution to 132 consignees in US, and 17 International consignees",
      "openfda": {
        "k_number": [
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          "K850908",
          "K802857",
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        "registration_number": [
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        ],
        "device_name": "Device, Microtiter Diluting/Dispensing",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.2500",
        "device_class": "1"
      }
    }
  ]
}