{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "New York",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90817",
      "recalling_firm": "DICOM Grid, Inc. d/b/a Ambra Health",
      "address_1": "450 Park Ave S Fl 10-111",
      "address_2": "N/A",
      "postal_code": "10016-7320",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Domestic: AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MS, MO, NE, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, DC, & PR.",
      "recall_number": "Z-1818-2022",
      "product_description": "Ambra PACS, Ambra ProViewer.  Software for use as a primary diagnostic and analysis tool for diagnostic images.",
      "product_quantity": "671 downloads",
      "reason_for_recall": "A race condition between the storage system and services database has the potential to revert edits made to patient information upon first ingestion of a study.",
      "recall_initiation_date": "20220623",
      "center_classification_date": "20220927",
      "report_date": "20221005",
      "code_info": "UDI-DI: AMBRHEALTHSOLUTIONS0; Software Version: 3.22.2.0 and 3.22.3.0."
    }
  ]
}