{
  "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": "Ongoing",
      "city": "Barrie",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88103",
      "recalling_firm": "Southmedic, Inc.",
      "address_1": "50 Alliance Blvd",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "U.S.: IL    O.U.S.: N/A",
      "recall_number": "Z-2141-2021",
      "product_description": "OxyMask O2 Adult REF OM-1125-14",
      "product_quantity": "160 cases (25 units per case) in U.S.",
      "reason_for_recall": "Potential for oxygen tubing to disconnect from mask or loosen.    Disconnected tubing results in a loss of device function and use of the device could result in inappropriate or a lack of oxygen delivery to the patient.",
      "recall_initiation_date": "20210525",
      "center_classification_date": "20210723",
      "report_date": "20210804",
      "code_info": "Model: OM-1125-14  Lot Number: W73887"
    }
  ]
}