{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tucson",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79631",
      "recalling_firm": "Accelerate Diagnostics Inc",
      "address_1": "3950 S Country Club Rd Ste 470",
      "address_2": "N/A",
      "postal_code": "85714-2240",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distributed to IL, TX, CA, SC, and DE.",
      "recall_number": "Z-1529-2018",
      "product_description": "Accelerate PhenoTest BC kit, Ref #10101018.  The firm name on the label is Accelerate Diagnostics, Tucson, AZ.    A multiplexed in-vitro diagnostic test intended for use with the Accelerate Pheno system.",
      "product_quantity": "95 kits",
      "reason_for_recall": "The kits may produce an elevated rate of false positive calls for the Staphylococcus aureus identification probe (SAU).",
      "recall_initiation_date": "20180314",
      "center_classification_date": "20180426",
      "termination_date": "20230117",
      "report_date": "20180502",
      "code_info": "Lot numbers 2880A, 2885A, 2886A, and 2887A, all with exp. date of 9/18/2018."
    }
  ]
}