{
  "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": "Elyria",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90108",
      "recalling_firm": "Invacare Corporation",
      "address_1": "1200 Taylor St",
      "address_2": "",
      "postal_code": "44035-6248",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to the following states: ALASKA  ARIZONA  CALIFORNIA  COLORADO  GEORGIA  IDAHO  IOWA  KANSAS  KENTUCKY  MICHIGAN  MINNESOTA  MISSOURI  NEW YORK  NORTH CAROLINA  OHIO  OKLAHOMA  PENNSYLVANIA  TENNESSEE",
      "recall_number": "Z-1369-2022",
      "product_description": "Invacare Platinum 5NXG Oxygen Concentrator, Model Numbers P5NXG1, P5NXGC1 (Canada specific model)",
      "product_quantity": "179 devices",
      "reason_for_recall": "Between March 2, 2021 and December 31, 2021, the product label used in production did not contain the \"Rx Only\" statement as required.",
      "recall_initiation_date": "20220610",
      "center_classification_date": "20220712",
      "report_date": "20220720",
      "code_info": "UDI-DI: 00841447112075    Serial Number Prefixes:   21FEXXXXXX 21JEXXXXXX  21GEXXXXXX 21KEXXXXXX  21HEXXXXXX 21LEXXXXXX  21IEXXXXXX",
      "more_code_info": ""
    }
  ]
}