{
  "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": "Boonton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89314",
      "recalling_firm": "PTW NORTH AMERICA CORPORATION",
      "address_1": "6 Mars Ct Rm Unit 5",
      "address_2": "N/A",
      "postal_code": "07005-9309",
      "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 in the state of CO.",
      "recall_number": "Z-0479-2022",
      "product_description": "Software BeamAdjust version 2.2, Catalog No: S070009  Software VeriSoft version 8.0, Catalog No: S080032",
      "product_quantity": "1 unit",
      "reason_for_recall": "When a measurement with a PTW detector array is performed with the software BeamAdjust 2.2 or VeriSoft 8.0, a measurement error can occur under specific conditions. This error can lead to a too-low or too-high measured absolute dose which affects patient plan verification results",
      "recall_initiation_date": "20210827",
      "center_classification_date": "20220111",
      "termination_date": "20240209",
      "report_date": "20220119",
      "code_info": "S/N :AU2001094-1  UDI: EPTWS0700090  VeriSoft ;EPTWS0700090  BeamAdjust"
    }
  ]
}