{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Flanders",
      "address_1": "62 Flanders-Bartley Rd",
      "reason_for_recall": "The bottle assemblies were manufactured with a quality issue where in some cases the smaller diameter opening on both IMMULITE 2000 and IMMULITE 2000XPi Water Bottles and Liquid Waste Bottles is undersized and/or deformed, preventing the cap from closing or fastening securely to the bottle.",
      "address_2": "",
      "product_quantity": "231 bottles",
      "code_info": "(Liquid Waste Bottle) -Product Code/ Catalog #10291587",
      "center_classification_date": "20150523",
      "distribution_pattern": "Worldwide Distribution.",
      "state": "NJ",
      "product_description": "Liquid Waste Bottle, Catalog#10291587.    The Immulite 2000 systems are continuous random-access instruments that perform chemiluminescent immunoassays. These instruments use serum, plasma, or urine samples for in vitro diagnostic testing.",
      "report_date": "20150603",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions Diagnostics",
      "recall_number": "Z-1659-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71022",
      "termination_date": "20180116",
      "more_code_info": "",
      "recall_initiation_date": "20150305",
      "postal_code": "07836-4715",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}