{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "East Walpole",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99446",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "address_1": "333 Coney St",
      "address_2": "",
      "postal_code": "02032-1516",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the state of CA and the country of Italy.",
      "recall_number": "Z-2976-2026",
      "product_description": "Beckman Coulter, Emit 2000 Quinidine Assay  REF: OSR4Q229  Contents: R1: 2 x 23 mL;R2 2x13 mL",
      "product_quantity": "55 units",
      "reason_for_recall": "Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine measurements, creating risk of sub-optimal patient treatment, including potential life-threatening cardiac arrhythmias or inadequate antimalarial therapy.",
      "recall_initiation_date": "20260713",
      "center_classification_date": "20260817",
      "report_date": "20260826",
      "code_info": "Lots: 2597, 2627, 2709/UDI: 00842768023293",
      "more_code_info": ""
    }
  ]
}