{
  "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,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Middletown",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96488",
      "recalling_firm": "Fisher Diagnostics",
      "address_1": "8365 Valley Pike",
      "address_2": "",
      "postal_code": "22645-1905",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to: PA and OUS Foreign country of: United Arab Emirates.",
      "recall_number": "Z-1503-2025",
      "product_description": "Pacific Hemostasis Thromboplastin-D, 10 ml. Used in performing one-stage prothrombin time test and factor assays.",
      "product_quantity": "1,699 units",
      "reason_for_recall": "The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.",
      "recall_initiation_date": "20250306",
      "center_classification_date": "20250331",
      "report_date": "20250409",
      "code_info": "Catalog No. 100357; UDI: 00845275000798665150270131100357; Lot No. 665150; Exp. Date 01/31/2027.",
      "more_code_info": ""
    }
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}