{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98979",
      "recalling_firm": "Accriva Diagnostics, Inc.",
      "address_1": "6260 Sequence Dr",
      "address_2": "",
      "postal_code": "92121-4358",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "Worldwide - US Nationwide  distribution including in the states of AL, AR, AZ, CA, FL, GA, \tID, IL, IN, KY, MA, MD, MI, MN, MO, MT, NC, NJ, NM, NY, OH, OK, PA, SC, TN, TX, VA, VT, WA, \tWI, WV and the countries of Canada, Hong Kong, Spain.",
      "recall_number": "Z-2460-2026",
      "product_description": "directCHECK ACT-LR whole blood quality control, level 2  Model/Catalog Number: DCGLR-2",
      "product_quantity": "6060",
      "reason_for_recall": "Assayed Whole blood control contains labeling with incorrect performance range.",
      "recall_initiation_date": "20260430",
      "center_classification_date": "20260616",
      "report_date": "20260624",
      "code_info": "Lot #: A6DLA001  Unique Device Identifier: 10711234170373",
      "more_code_info": ""
    }
  ]
}