{
  "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-2290-2019",
      "product_description": "IMMULITE 2000 Progesterone; Models US: L2KPW2, L2KPW6 and OUS: L2KPW2(D), L2KPW6(D);  SMN Numbers US: 10901873, 10901874 and OUS 10381181, 10381170",
      "product_quantity": "6633 (4753 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": "US kit lots 510 and above; OUS kit lots D510 and above;  UDI: US 00630414167718, 00630414167510 and OUS 00630414961972, 00630414961989"
    }
  ]
}