{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Torrance",
      "address_1": "20101 S Vermont Ave",
      "reason_for_recall": "Shimadzu Corporation is recalling the Shimadzu Mobile X-ray Sytems (MUX-100 and MUX-100H) because the connecting metal plate which connects the main chassis and the column of MUX-100 may crack.",
      "address_2": "",
      "product_quantity": "56 units",
      "code_info": "Serial No.    0262P70907  0262P70908  0262P70909  0262P70910  0262P71001  0262P71002  0262P71003  0262P71004  0262P71005  0262P71006  0162Z01901  0162Z01902  0162Z01903  0162Z01904  0162Z01905  0162Z02002  0162Z02003  0162Z02004  0162Z02005  0162Z02006  0162Z02007  0162Z02008  0162Z02009  0162Z02101  0162Z02108  0162Z02204  0162Z02205  0162Z02302  0162Z02303  0162Z02304  0162Z02305  0162Z02306  0162Z02307  0162Z02308  0162Z02309  0162Z02310  0262Z00205  0262Z00206  0262Z00207  0262Z00208  0262Z00209  0262Z00210  0262Z00307  0262Z00308  0262Z00309  0262Z00310  0262Z00401  0262Z00402  0262Z00403  0262Z00404  0262Z00610  0262Z00701  0262Z00702  0262Z00703  0262Z00704  0262Z00705",
      "center_classification_date": "20140306",
      "distribution_pattern": "USA Nationwide Distribution",
      "state": "CA",
      "product_description": "Mobile X-ray System, Model: MUX-100, MUX-100H    Product Usage:  The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannnot move and/or of outpatients in emergency",
      "report_date": "20140312",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Shimadzu Medical Systems",
      "recall_number": "Z-1150-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67353",
      "termination_date": "20150625",
      "more_code_info": "",
      "recall_initiation_date": "20131115",
      "postal_code": "90502-1328",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}