{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70149",
      "recalling_firm": "Shape Medical Systems, Inc",
      "address_1": "5000 Township Pkwy",
      "address_2": "N/A",
      "postal_code": "55110-5852",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of AZ, FL, GA, MA, MN, NJ. NY, PA, TX, and WI.",
      "recall_number": "Z-1060-2015",
      "product_description": "Shape-HF Cardiopulmonary Testing System Disposable Patient Interface (DPI).   Part Number 0004-4001.    The Shape-HF Cardiopulmonary Exercise Testing System is a stationary device that monitors parameters during laboratory or clinical conditions.",
      "product_quantity": "564 devices",
      "reason_for_recall": "This recall has been initiated because use of the impacted DPIs could result in erroneous testing results potentially leading to incorrect diagnosis and incorrect treatment. The magnitude of error for VO2 or VCO2 parameters could be approximately 20% with use of the impacted product.",
      "recall_initiation_date": "20141223",
      "center_classification_date": "20150205",
      "termination_date": "20150414",
      "report_date": "20150211",
      "code_info": "Lot Numbers: 1412001, 1412002, 1412003 and 1412004"
    }
  ]
}