{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Baar",
      "state": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97451",
      "recalling_firm": "Schiller, Ag",
      "address_1": "Altgasse 68",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of MT, WI, IL.",
      "recall_number": "Z-2672-2025",
      "product_description": "Argus PB-3000, Reference Numbers:  1A.701307,3.921002, 3.921030,3.921031, 3.921006",
      "product_quantity": "266 units",
      "reason_for_recall": "Vital sign monitoring instrument may trigger an error message  during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.",
      "recall_initiation_date": "20250808",
      "center_classification_date": "20250929",
      "report_date": "20251008",
      "code_info": "REF: 1A.701307: UDI- 07613365003024 REF: 3.921002, UDI: 07613365001914 REF: 3.921030, UDI: 07613365003468 REF: 3.921031: UDI: 07613365003475 REF: 3.921006, UDI: 07613365000115 Affected Serial Numbers: 7010.000160 and lower, 7012.000356 and lower, 7013.000256 and lower, 7014.000152 and lower"
    }
  ]
}