{
  "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": "2026-08-19",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99261",
      "recalling_firm": "BioFire Diagnostics, LLC",
      "address_1": "515 S Colorow Dr",
      "address_2": "",
      "postal_code": "84108-1248",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "U.S. Nationwide distribution in the states of AL, AR, IA, IL, KS, LA, MN, MO, TX, and WI.",
      "recall_number": "Z-2936-2026",
      "product_description": "BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742  UDI code: 00815381020529    PCR-based multiplexed nucleic acid test, in vitro diagnostic",
      "product_quantity": "2,370 pouches (79 kits)",
      "reason_for_recall": "Due to increase in false negative results",
      "recall_initiation_date": "20260624",
      "center_classification_date": "20260812",
      "report_date": "20260819",
      "code_info": "Part Number: 423742 UDI-DI code: 00815381020529 Pouch Lot: 3VLB25 Kit Lot: 1872125",
      "more_code_info": ""
    }
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}