{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Phoenix",
      "address_1": "4530 E Muirwood Dr",
      "reason_for_recall": "A software error caused the window/level to become the same in one series regardless if the image had different levels; image results have a washed-out grey appearance.",
      "address_2": "Ste. 113",
      "product_quantity": "209",
      "code_info": "",
      "center_classification_date": "20170118",
      "distribution_pattern": "U.S. distribution to the following; TX, FL, NE, CA, WI, AZ, NH, MO, MA, CO, PA, NV, PR, IL, OH, NY, MD, NJ, MN, MI, CT, VA, GA, UT, KS, WA, MI, HI.    Foreign distribution to the following; Canada, Spain, Israel, Singapore, Kosovo, Austria, Brazil, Malaysia, Australia.",
      "state": "AZ",
      "product_description": "Ambra PACS    UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R  Software Version Number: V3.16.13.0    Intended for use as a primary diagnostic and analysis tool for diagnostic images.",
      "report_date": "20170125",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "DICOM GRID INC",
      "recall_number": "Z-1045-2017",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "76187",
      "termination_date": "20170407",
      "more_code_info": "",
      "recall_initiation_date": "20161216",
      "postal_code": "85048-7639",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}