{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Hazelwood",
      "address_1": "595 Anglum Rd",
      "reason_for_recall": "Missing desiccant.",
      "address_2": "",
      "product_quantity": "57 cartons",
      "code_info": "Batch/Lot: 245057043 Exp. Date 19JUN2019",
      "center_classification_date": "20180817",
      "distribution_pattern": "US Nationwide Distribution in the states of AK, AL, AR, AZ, CA, CO, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NY, OH, OK, OR, PA, SC, TN, TX, UT. VA. VT. WA. WI, and WV",
      "state": "MO",
      "product_description": "bioM¿rieux VITEK 2 NH ID Test Kit    Product Usage:  Is an automated system consisting of instruments, software and reagent cards designed for the ID and antimicrobial susceptibility testing of bacteria and yeast.",
      "report_date": "20180829",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomerieux Inc",
      "recall_number": "Z-2874-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80491",
      "termination_date": "20210713",
      "more_code_info": "",
      "recall_initiation_date": "20180123",
      "postal_code": "63042-2320",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}