{
  "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": "Vaxjo",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90446",
      "recalling_firm": "Arcoma AB",
      "address_1": "Annavagen 1",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of NM, DE, TX, VT, FL, MO, UT, PA, OR, IN, RI, MI, IL, LA, OH, CO, SC, VA, WA, CA, AZ, NV, AR and the country of Canada.",
      "recall_number": "Z-1331-2022",
      "product_description": "Omnera 400T Digital Radiographic System",
      "product_quantity": "71 systems",
      "reason_for_recall": "There is the  potential  for the X-Ray system to short circuit due to  an ingress of liquid in the display handles which may result in uncontrolled movement of the Overhead Tube Crane (OTC).",
      "recall_initiation_date": "20210505",
      "center_classification_date": "20220705",
      "report_date": "20220713",
      "code_info": "UDI/DI:07350008750050;  2001-2003, 2006-2044, 2046-2056, 2118-2126, 2128-2131, 2134-2160, 2164-2175, 2177-2195, 2197-2208, 2210-2212, 2214-2224, 2226-2236.",
      "more_code_info": ""
    }
  ]
}