{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "102757",
      "product_res_number": "Z-0177-2012",
      "event_date_initiated": "2011-07-08",
      "event_date_posted": "2011-11-09",
      "recall_status": "Terminated",
      "event_date_terminated": "2013-12-10",
      "res_event_number": "59425",
      "product_code": "KPT",
      "k_numbers": [
        "K071396"
      ],
      "product_description": "Capintec CRC 25 PET, item number 5130-3217 with Software Revisions 2.01 and 2.02\n\nPET dose calibrator",
      "code_info": "New units with serial numbers 270439 through 270506, consecutively, and repair units with serial numbers 270210, 270196, 270014, and 270333.",
      "firm_fei_number": "2518443",
      "recalling_firm": "Capintec Inc",
      "address_1": "620 Alpha Dr",
      "city": "Pittsburgh",
      "state": "PA",
      "postal_code": "15238",
      "additional_info_contact": "412-963-1988",
      "reason_for_recall": "Software error in Rev. 2.01 and Rev 2.02 for Capintec CRC 25PET",
      "root_cause_description": "Software design",
      "action": "Capintec, Inc. sent a Software Error Alert letter dated July 8, 2011, to all affected consignees.  The letter identified the product, the problem, and the action to be taken by the customer.   Customers were instructed to contac their Capintec Customer Support Representative to receive a software upgrade.  \n\nFor questions call Capintec Customer Support at 1-800-631-3826.",
      "product_quantity": "69",
      "distribution_pattern": "Worldwide distribution - United States including CA, FL, IL, MA, NJ, OK, PA, and VA; and internationally to Brazil, China, India, Indonesia, Italy, Japan, Korea, South Korea, and Turkey.",
      "openfda": {
        "k_number": [
          "K841785",
          "K090296",
          "K002833",
          "K935539",
          "K931657",
          "K813065",
          "K192199",
          "K013548",
          "K943072",
          "K770515",
          "K850838",
          "K842540",
          "K042746",
          "K011493",
          "K020150",
          "K071396",
          "K142325",
          "K880272",
          "K884312",
          "K141413",
          "K811320",
          "K841786",
          "K813379",
          "K010417",
          "K850815",
          "K013689",
          "K162394",
          "K905796",
          "K842570",
          "K841787",
          "K101452",
          "K030066"
        ],
        "registration_number": [
          "2518443",
          "3009694288"
        ],
        "fei_number": [
          "2518443",
          "3009694288"
        ],
        "device_name": "Calibrator, Dose, Radionuclide",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.1360",
        "device_class": "2"
      }
    }
  ]
}