{
  "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": "Boca Raton",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86241",
      "recalling_firm": "Office Depot Inc",
      "address_1": "6600 N Military Trl # N203r",
      "address_2": "N/A",
      "postal_code": "33496-2434",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "nationwide",
      "recall_number": "Z-3024-2020",
      "product_description": "JINYINSHAN, KN95 PROTECTIVE MASK P1, 20 pieces",
      "product_quantity": "25,360 masks",
      "reason_for_recall": "Test results revealed that the KN95 masks failed to filter greater than 95% of particulates.",
      "recall_initiation_date": "20200727",
      "center_classification_date": "20200928",
      "report_date": "20201007",
      "code_info": "SKU 4555098 & 8510447"
    }
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}