{
  "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": "Raleigh",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92619",
      "recalling_firm": "Digisonics, Inc",
      "address_1": "305 Church At North Hills St",
      "address_2": "N/A",
      "postal_code": "27609-2666",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution: AK, NH, WY, TX, NE, CA, MD, TX, OR IA, IL, MO, OR, NY, UT, PA, MA, GA, VA, WA, WI, and Internationally to :Aruba",
      "recall_number": "Z-2214-2023",
      "product_description": "Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound reporting software",
      "product_quantity": "32 units",
      "reason_for_recall": "Software issue",
      "recall_initiation_date": "20230626",
      "center_classification_date": "20230720",
      "report_date": "20230726",
      "code_info": "UDI?DI 00857050006014, Versions 4.8.2 SP6 - 4.8.3",
      "more_code_info": ""
    }
  ]
}