{
  "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": "Mississauga",
      "state": "",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77528",
      "recalling_firm": "O-Two Medical Technologies, Inc.",
      "address_1": "7575 Kimbel Street",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) Canada, Europe Denmark and Finland",
      "recall_number": "Z-2705-2017",
      "product_description": "O-Two Adult Ventilation Timer,  MODEL #(s): 01BM1000-CS, 01BM3201-MOTP-CS, 01BM3201-MOTL-CS, CATALOG #(s): 01BM1000 ---   INTENDED USE: The Adult Ventilation Timer is intended to guide the rescuer to provide ventilations at a rate appropriate for adult patients",
      "product_quantity": "4382 units (4082 units distributed USA)",
      "reason_for_recall": "Malfunction of an O-Two Adult Ventilation Timer, where the flash rate of the malfunctioning device was reported to be twice that of the rate noted on the label.",
      "recall_initiation_date": "20150623",
      "center_classification_date": "20170710",
      "termination_date": "20170901",
      "report_date": "20170719",
      "code_info": "Lot #s:  079810;   078734, 081071, 140411, 141117, 140719, 140506, 130117 Expiration date: Jul.2016",
      "more_code_info": ""
    }
  ]
}