{
  "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": "2026-09-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "216787",
      "product_res_number": "Z-0500-2026",
      "event_date_initiated": "2025-10-21",
      "event_date_posted": "2025-11-13",
      "recall_status": "Open, Classified",
      "res_event_number": "97863",
      "product_code": "JOZ",
      "k_numbers": [
        "K141427"
      ],
      "product_description": "VerifyNow PRUTest Platelet Reactivity Test REF 85225\nUDI-DI code: 10711234150078\n\nThe 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.",
      "code_info": "Catalog Number: 85225\nUDI-DI code: 10711234150078\nLot Number: WP1559-01",
      "firm_fei_number": "2250033",
      "recalling_firm": "Accriva Diagnostics, Inc.",
      "address_1": "6260 Sequence Dr",
      "city": "San Diego",
      "state": "CA",
      "postal_code": "92121-4358",
      "additional_info_contact": "Paula Morgan\n858-263-2590",
      "reason_for_recall": "Due to an device without a premarket clearance being incorrectly package and distributed.",
      "root_cause_description": "Under Investigation by firm",
      "action": "On 10/21/2025, the firm sent via email an \"Urgent Medical Device Recall\" Letter to customers informing them that Accriva Diagnostics, Inc. has identified that a small number of VerifyNow PRUTest Platelet Reactivity Test (85225) cartridge pouches from lot WP1559-01 may contain VerifyNow P2Y12 Test cartridges. VerifyNow P2Y12 Test cartridges are not cleared by the US-FDA for use in the United States.\n\nCustomers are instructed to:\n1. Please forward this communication to those within your organization who need to become aware of this matter and verify they understand the procedure and can complete the enclosed forms.\n2. In addition, forward the enclosed customer notification to all other organizations where affected devices may have been transferred to.\n3. Please check your inventory to determine if you have any boxes of VerifyNow PRU Platelet Reactivity Test (85225), lot number WP1559-01. If you have this product in stock, do NOT use.\n4. Please sort through your inventory to identify if your inventory is affected.\n5. Please destroy all impacted boxes and document on the enclosed form.\n6. Please read the instructions on the Tracking Form and complete and return the form to Accriva Diagnostics, Inc.\n7. If you have questions regarding replacement product, please contact Customer Service at 1-800-955-9525 or e-mail customerservice.na@werfen.com.",
      "product_quantity": "125 boxes (3,125 tests)",
      "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.",
      "openfda": {
        "k_number": [
          "K790769",
          "K770395",
          "K122162",
          "K780047",
          "K051231",
          "K800146",
          "K032951",
          "K012701",
          "K140893",
          "K060489",
          "K191364",
          "K962426",
          "K862302",
          "K011337",
          "K013596",
          "K992531",
          "K163274",
          "K141427",
          "K990398",
          "K042423",
          "K023761",
          "K103555",
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          "K781807",
          "K851669",
          "K800432",
          "K940792",
          "K780285",
          "K954997",
          "K781693",
          "K050265",
          "K970505",
          "K012723",
          "K760893",
          "K041502",
          "K002885",
          "K181777",
          "K791577"
        ],
        "device_name": "System, Automated Platelet Aggregation",
        "medical_specialty_description": "Hematology",
        "regulation_number": "864.5700",
        "device_class": "2",
        "registration_number": [
          "1000487132",
          "3019849102",
          "9610806",
          "3002807408",
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        ],
        "fei_number": [
          "1000487132",
          "2250033",
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          "3019849102",
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          "3005739529",
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          "1219343",
          "3003601075",
          "3003455467",
          "1618982",
          "3001644026"
        ]
      }
    }
  ]
}