{
  "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": "Terminated",
      "city": "Lexington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82187",
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "address_1": "81 Hartwell Ave Ste 300",
      "address_2": "N/A",
      "postal_code": "02421-3160",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1040-2019",
      "product_description": "Fujifilm FDR Go PLUS,  Mobile X-Ray System    Product Usage:  This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography (DR)>",
      "product_quantity": "56 units",
      "reason_for_recall": "FUJIFILM Medical Systems U.S.A., Inc., Modality Systems became aware of the possibility that the braking mechanism might not be engaged in all cases when the driving handle has been released.",
      "recall_initiation_date": "20190115",
      "center_classification_date": "20190321",
      "termination_date": "20201008",
      "report_date": "20190327",
      "code_info": "Serial Numbers: MQ0001281001 through MQ0001285004"
    }
  ]
}