{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Norwood",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90432",
      "recalling_firm": "Siemens Healthcare Diagnostics Inc",
      "address_1": "2 Edgewater Dr",
      "address_2": "",
      "postal_code": "02062-4637",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AL  CA  CO  FL  IA  ID  KS  NM  OK  TX",
      "recall_number": "Z-1372-2022",
      "product_description": "epoc BGEM Test Card  25 Test Cards/box. In vitro diagnostic device for the quantitative testing of samples of heparinized or un-anticoagulated arterial, venous or capillary whole blood  Product Siemens SMN#/Model #: 10736515",
      "product_quantity": "263 Boxes",
      "reason_for_recall": "Discrepant (low bias) pO2 results, could be an incorrect diagnosis of hypoxemia and initiation of unnecessary or inappropriate respiratory support.",
      "recall_initiation_date": "20220601",
      "center_classification_date": "20220712",
      "report_date": "20220720",
      "code_info": "UDI-DI: 00809708121860  Lot Number: 11-22005-50   Exp. Date: 22-June-2022",
      "more_code_info": ""
    }
  ]
}