{
  "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": "Uppsala",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83402",
      "recalling_firm": "Phadia Ab",
      "address_1": "Rapsgatan Plant",
      "address_2": "Rapsgatan 7",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of  CA  CO  FL  GA  HI  IL  IN  KS  KY  MA  MD  MI  MO  NC  NJ  NV  NY  OH  OK  OR  PA  TN  TX  UT  VA  WA",
      "recall_number": "Z-2397-2019",
      "product_description": "Phadia\" 1000  Model # 12-3800-01    Product Usage:  The instrument is fully integrated and automated instrument including software for immunodiagnostic testing. The instrument is designed to handle all steps from sample and reagent handling to processing of results.",
      "product_quantity": "387 Instruments",
      "reason_for_recall": "code 7-102  Liquid Sensor Error",
      "recall_initiation_date": "20190709",
      "center_classification_date": "20190826",
      "termination_date": "20220712",
      "report_date": "20190904",
      "code_info": "All Serial Numbers;   Unique Device Identifier (UDI): 07333066001005"
    }
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}