{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Brampton",
      "state": "Ontario",
      "country": "Canada",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82178",
      "recalling_firm": "O-Two Medical Technologies, Inc.",
      "address_1": "45A Armthorpe Road",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states:  AZ, CA, CO, FL, OH, PA, TX, and VA.",
      "recall_number": "Z-0976-2019",
      "product_description": "e500 Automatic Transport Ventilator,  Model Number 01EVE500",
      "product_quantity": "136",
      "reason_for_recall": "There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main board causing the screw to rub against the bottom side of the board, wearing away the insulation layer and creating a short circuit.",
      "recall_initiation_date": "20190212",
      "center_classification_date": "20190404",
      "termination_date": "20230629",
      "report_date": "20190410",
      "code_info": "EV50001 to EV50148"
    }
  ]
}