{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tarrytown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83349",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "address_1": "511 Benedict Ave",
      "address_2": "N/A",
      "postal_code": "10591-5005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Global distribution.  US Nationwide.",
      "recall_number": "Z-2289-2019",
      "product_description": "IMMULITE 1000 Progesterone, Model LKPW1, SMN Number 10381128",
      "product_quantity": "4780 (6266 additional as of 1/13/20)",
      "reason_for_recall": "There is a potential for low discordant progesterone results on a subset of patient samples.  A falsely low progesterone result may lead to the consideration for additional progesterone  supplementation.",
      "recall_initiation_date": "20190710",
      "center_classification_date": "20190817",
      "termination_date": "20240528",
      "report_date": "20190828",
      "code_info": "kit lots 0259 and above; UDI: 00630414985732"
    }
  ]
}