{
  "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-1269-2014",
      "product_description": "AMS AST For the In vitro quantitative determination of AST in serum     Quantitative determination of AST in serum.",
      "product_quantity": "116 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, 80146. Lot codes: 131083, 131084, 131085, 131086, 131087, 131088, 131089, 1310810, 1310811, 1310812, 1310813, 1310814, 1310815, 141081."
    }
  ]
}