{
  "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": "East Walpole",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68537",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc",
      "address_1": "333 Coney St",
      "address_2": "N/A",
      "postal_code": "02032-1516",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide and the countries of Canada, Argentina, China, Colombia, Korea,  Malyasia, New Zealand, Mexico, Guatemala, and Singapore.",
      "recall_number": "Z-1927-2014",
      "product_description": "Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing ADVIA Centaur Acid Reagent bottles, lot number: 454778  Kit Catalog Number: 112219  SMN: 10310026    Intended Use: In vitro diagnostic use. Acid Regent is a component of the ADVIA Centaur and ADVIA Centaur XP instruments",
      "product_quantity": "3,839 kits",
      "reason_for_recall": "Swollen acid bottles due to a trace metal contamination in the Acid Reagent bottles",
      "recall_initiation_date": "20140602",
      "center_classification_date": "20140626",
      "termination_date": "20150205",
      "report_date": "20140702",
      "code_info": "Kit Lot Number: 454779  Exp. Date: 28 February, 2015"
    }
  ]
}