{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Hazelwood",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63019",
      "recalling_firm": "Biomerieux Inc",
      "address_1": "595 Anglum Rd",
      "address_2": "N/A",
      "postal_code": "63042-2320",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide)-including DC and the states of CA, CO, CT, FL, GA, IL, IN, KY, LA, MO, NC, NJ, NY, OH, OR, PA, RI, SC, TX, and WI, and the country of Canada.",
      "recall_number": "Z-0023-2013",
      "product_description": "PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC.    Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.",
      "product_quantity": "350 systems",
      "reason_for_recall": "The instrument may not dispense the specimen onto the pre-poured media resulting in a false negative result.",
      "recall_initiation_date": "20120828",
      "center_classification_date": "20121009",
      "termination_date": "20140904",
      "report_date": "20121017",
      "code_info": "Serial numbers AS180-00001 to AS180-00376."
    }
  ]
}