{
  "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": "Torrance",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89596",
      "recalling_firm": "Shimadzu Medical Systems",
      "address_1": "20101 S Vermont Ave",
      "address_2": "",
      "postal_code": "90502-1328",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: AK, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, WA, and WV.    O.U.S.: N/A",
      "recall_number": "Z-0869-2022",
      "product_description": "MODEL: X-RAY TV SYSSTEM SONIALVISION safire17",
      "product_quantity": "12 systems",
      "reason_for_recall": "It was found that the irradiated x-ray may exceed the xray radiation dose rate specified in CFR 1020.32 in some specific case of fluoroscopic mode due to inadequate adjusting criteria in installation.",
      "recall_initiation_date": "20220110",
      "center_classification_date": "20220406",
      "report_date": "20220413",
      "code_info": "Model: SonialVision safire:  Generator Number: D150-40  Serial Numbers:  3M5249D41006  3M5249D2A004  3M5249D34001  3M5249D37006  3M5249D32012  3M5249D35002  3M5249D1C013  3M5249D31009  3M5249D29002  3M5249D33003  3M5249D2C004  3M5249D22013",
      "more_code_info": ""
    }
  ]
}