{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "West Chester",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82468",
      "recalling_firm": "Aniara Diagnostica LLC",
      "address_1": "7768 Service Center Dr",
      "address_2": "N/A",
      "postal_code": "45069-2442",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed to accounts in MI and PA.",
      "recall_number": "Z-1190-2019",
      "product_description": "BIOPHEN LMWH Control C4, REF 224201",
      "product_quantity": "3 units",
      "reason_for_recall": "The manufacturer packaged incorrect versions of the Instructions for Use into specific lots for three device product codes.",
      "recall_initiation_date": "20190319",
      "center_classification_date": "20190417",
      "termination_date": "20190712",
      "report_date": "20190424",
      "code_info": "Lots F1701555P4"
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}