{
  "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": "95088",
      "product_res_number": "Z-0167-2011",
      "event_date_initiated": "2010-09-20",
      "event_date_posted": "2010-10-28",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-07-05",
      "res_event_number": "56975",
      "product_code": "KPT",
      "product_description": "Captus 3000 Thyroid Uptake System with Portable Stand option.  Capintec item number 5430-2130, serial numbers:  91001, 91003 through 91010. Manufactured by Capintec, Inc, Pittsburgh, PA.",
      "code_info": "Capintec item number 5430-2130, serial numbers:  91001, 91003 through 91010",
      "firm_fei_number": "2518443",
      "recalling_firm": "Capintec Inc",
      "address_1": "620 Alpha Dr",
      "city": "Pittsburgh",
      "state": "PA",
      "postal_code": "15238",
      "additional_info_contact": "Art Hall\n201-825-9500",
      "reason_for_recall": "The spring arm on portable stand may have been over tightened during assembly, which may result in failure. If the spring arm fails, it will not balance the collimator weight, and the arm will drop to the lowest position.",
      "root_cause_description": "Employee error",
      "action": "Capintec issued an Alert letter to all customers identifying the affected device, informing them of the problem and what actions are to be taken by customers. Capintec will send a replacement arm for the system, which is to be installed by the customer using included instructions. The firm included a correction acknowledgement form to be completed and returned by the customer.\nCustomers can contact Capintec concerning this recall at 201 825-9500.",
      "product_quantity": "9 units",
      "distribution_pattern": "Worldwide Distribution: USA in the states of NC and TN, and in the countries of  Pakistan, Paraguay, Portugal, Saudi Arabia, and Spain.",
      "openfda": {
        "k_number": [
          "K142325",
          "K013689",
          "K880272",
          "K010417",
          "K813065",
          "K020150",
          "K042746",
          "K162394",
          "K770515",
          "K101452",
          "K850838",
          "K811320",
          "K943072",
          "K841786",
          "K842540",
          "K884312",
          "K905796",
          "K931657",
          "K011493",
          "K850815",
          "K071396",
          "K013548",
          "K141413",
          "K030066",
          "K813379",
          "K841785",
          "K935539",
          "K090296",
          "K192199",
          "K841787",
          "K002833",
          "K842570"
        ],
        "registration_number": [
          "2518443",
          "3009694288"
        ],
        "fei_number": [
          "2518443",
          "3009694288"
        ],
        "device_name": "Calibrator, Dose, Radionuclide",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.1360",
        "device_class": "2"
      }
    }
  ]
}