{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97863",
      "recalling_firm": "Accriva Diagnostics, Inc.",
      "address_1": "6260 Sequence Dr",
      "address_2": "",
      "postal_code": "92121-4358",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - U.S. Nationwide distribution in the states of AK, CA, FL, IA, IL, MD, MI, NY, SD, and TX. The countries of Hong Kong, Japan.",
      "recall_number": "Z-0500-2026",
      "product_description": "VerifyNow PRUTest Platelet Reactivity Test REF 85225  UDI-DI code: 10711234150078    The VerifyNow PRUTest is a whole blood test used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade.",
      "product_quantity": "125 boxes (3,125 tests)",
      "reason_for_recall": "Due to an device without a premarket clearance being incorrectly package and distributed.",
      "recall_initiation_date": "20251021",
      "center_classification_date": "20251113",
      "report_date": "20251119",
      "code_info": "Catalog Number: 85225 UDI-DI code: 10711234150078 Lot Number: WP1559-01",
      "more_code_info": ""
    }
  ]
}