{
  "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-0551-2019",
      "product_description": "Captus 700 Thyroid Uptake System, Model # 5430-3137 and 5430-3138",
      "product_quantity": "65",
      "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 700004 through 700018.  Serial Numbers 700019 through 700086 as of 1/15/19."
    }
  ]
}