{
  "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": "Weston",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67599",
      "recalling_firm": "AMS Diagnostics, LLC",
      "address_1": "1790 N Commerce Pkwy",
      "address_2": "N/A",
      "postal_code": "33326-3204",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide Distribution including FL, GA, MD, CA, NC, MA, SC, WY, and TX.",
      "recall_number": "Z-1267-2014",
      "product_description": "AMS BUN UREA NITROGEN For the In vitro quantitative determination of Urea Nitrogen in serum    Quantitative determination of Bun in serum.",
      "product_quantity": "167 kits",
      "reason_for_recall": "Marketing the devices outside 510(k) requirements",
      "recall_initiation_date": "20140211",
      "center_classification_date": "20140321",
      "termination_date": "20160929",
      "report_date": "20140402",
      "code_info": "Model Numbers: 40072, 40146, 81046. Lot codes: 131083, 131084, 131085, 131086, 131087, 131088, 131089, 1310810, 1310811, 1310812, 1310813, 1310814, 1310815, 141081."
    }
  ]
}