{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Framingham",
      "address_1": "31 New York Ave",
      "reason_for_recall": "Discoloration of the acetaminophen enzyme reagent (R1), generates a high calibration factor and erratic control recovery.",
      "address_2": "",
      "product_quantity": "1600 kits",
      "code_info": "Lot 41928UQ11 {exp 2013-01 -31 )",
      "center_classification_date": "20120627",
      "distribution_pattern": "Illinois",
      "state": "MA",
      "product_description": "MULTIGENT Acetaminophen for use with Architect/Aeroset  Cat. No. 2K99-20.    Assay is intended for the quantitative determination of acetaminophen in human serum or plasma.",
      "report_date": "20120704",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Sekisui Diagnostics Llc",
      "recall_number": "Z-1902-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62017",
      "termination_date": "20121114",
      "more_code_info": "",
      "recall_initiation_date": "20120529",
      "postal_code": "01701-8860",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}