{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "61761",
      "recalling_firm": "Accumetrics Inc",
      "address_1": "3985 Sorrento Valley Blvd Ste B",
      "address_2": "N/A",
      "postal_code": "92121-1497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1854-2012",
      "product_description": "VerifyNow System, part #85005-6H    Product Usage:  The VerifyNow P2Y12 assay device is a whole blood assay used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade. The VerifyNow System\u0019s intended for use with human whole blood and verify now test devices. The system should be operated by healthcare professionals trained on use of the system and in accordance with institution and policies and procedures. Accumetrics respresentatives will assist your institution in the installation of the system and operations of the operator.",
      "product_quantity": "1,167 units total",
      "reason_for_recall": "The recall was initiated by Accumetrics because of a field correction to the VerifyNow System; specifically the results reported when running the VerifyNow P2Y12 Test.  Currently the VerifyNow P2Y12 Test reports three values:  PRU, BASE and % Inhibition.  The change implemented is the elimination of the BASE and % Inhibition results.  There will be no change to the reporting of the PRU result whic",
      "recall_initiation_date": "20120206",
      "center_classification_date": "20120621",
      "termination_date": "20121127",
      "report_date": "20120627",
      "code_info": "Not available"
    }
  ]
}