{
  "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": "Parsippany",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97596",
      "recalling_firm": "Diagnostica Stago, Inc.",
      "address_1": "5 Century Dr",
      "address_2": "",
      "postal_code": "07054-4607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution- US Nationwide and the country of Canada.",
      "recall_number": "Z-0205-2026",
      "product_description": "Product: STA Liatest D-Di;  REF: 00515;",
      "product_quantity": "12740 units",
      "reason_for_recall": "A potential risk of underestimation of D-Dimer (D-Di) levels with the two listed lots.",
      "recall_initiation_date": "20250912",
      "center_classification_date": "20251016",
      "report_date": "20251022",
      "code_info": "REF: 00515; UDI-DI: 03607450005158; Lot numbers: 271382, 271411; Expiration 09/30/2025;",
      "more_code_info": ""
    }
  ]
}