{
  "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": "Ongoing",
      "city": "Turku",
      "state": "N/A",
      "country": "Finland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82064",
      "recalling_firm": "PerkinElmer Life and Analytical Sciences, Wallac, OY",
      "address_1": "Mustionkatu 6",
      "address_2": "P.O. Box 10",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution. and countries of  Austria, Bolivia, UK,  Switzerland,Thailand, Finland.",
      "recall_number": "Z-1237-2019",
      "product_description": "DELFIA¿ hCG Kit, In Vitro Diagnostic for the determination of human gonadotropin (hCG)  Product Code: A007-101 - Product Usage: Quantitative determination of human gonadotrophin (hCG) in serum.",
      "product_quantity": "31 kits (10 in US, 21 in ROW)",
      "reason_for_recall": "hCG analyte concentrations may be decreased up to 15- 20% at the lower measuring range of hCG concentrations.",
      "recall_initiation_date": "20190110",
      "center_classification_date": "20190426",
      "report_date": "20190508",
      "code_info": "Kit Lot Numbers: 664891, 666471, 666604  Pack Lot Numbers: 1066489101, 1066647101,1066660401  UDI:   (01)06438147009176(17)190430(10)664891  (01)06438147009176(17)190430(10)666471  (01)06438147009176(17)190430(10)666604"
    }
  ]
}