{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Florham Park",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81605",
      "recalling_firm": "Capintec Inc",
      "address_1": "7 Vreeland Road",
      "address_2": "N/A",
      "postal_code": "07932",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US nationwide distributed in the states of AR, AZ, CA, CO, CT, DC, FL, IA, IN, LA, MD, MI, MN, NC, NJ, OH, OK, PA, SC, SD, TX, VA, WI, WV, and countries of Argentina, Brazil, Canada, China, Cyprus, Greece, Hong Kong, India, Japan, South Korea, Vietnam.",
      "recall_number": "Z-0550-2019",
      "product_description": "Captus 3000 Thyroid Uptake System, Model # 5430-0076 and 5430-0077",
      "product_quantity": "385",
      "reason_for_recall": "There is a potential for the spring arm failure as a result of a broken tension rod (a component inside the arm).  A break in the tension rod can casue the collimator to fall downward to its lowest point of travel, approximately 25 inches from the ground.",
      "recall_initiation_date": "20181105",
      "center_classification_date": "20181204",
      "termination_date": "20200630",
      "report_date": "20181212",
      "code_info": "Serial Numbers 901100 through 901309.  Serial Numbers 901310 through 901965 as of 1/15/19."
    }
  ]
}