{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Tarrytown",
      "address_1": "511 Benedict Ave",
      "reason_for_recall": "24 minutes of incubation is required prior to processing patient samples and for the pretreatment solution to reach full equilibration when using pretreatment solution when using the pretreatment solution (LGFA) contained in the kit.",
      "address_2": "",
      "product_quantity": "525 units",
      "code_info": "SMN Number:10381403  Lot: 411  Expired: 2016-04",
      "center_classification_date": "20160916",
      "distribution_pattern": "Domestic: IL, FL, NY, OH, LA, MO, MA; International: Canada, others will be inserted",
      "state": "NY",
      "product_description": "IG1, IGF-I reagent, Catalog # LKGF1; For the quantitative measurement of insulin-like growth factor I (IGF-I) in serum or heparinized plasma.",
      "report_date": "20160928",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-2841-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73995",
      "termination_date": "20170420",
      "more_code_info": "",
      "recall_initiation_date": "20160415",
      "postal_code": "10591-5005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}