{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "New York",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86431",
      "recalling_firm": "THREAD COUNSEL INC DBA LAWS OF MOTION",
      "address_1": "175 Varick St",
      "address_2": "N/A",
      "postal_code": "10014-4604",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to accounts in New York",
      "recall_number": "Z-0296-2021",
      "product_description": "LOM Disposable Surgical Gowns/Medical Gowns, Single-Use",
      "product_quantity": "2.4 million",
      "reason_for_recall": "Medical gowns distributed to customers did not include appropriate labeling, and some gowns may not meet FDA's standards for surgical gowns.",
      "recall_initiation_date": "20200917",
      "center_classification_date": "20201025",
      "report_date": "20201104",
      "code_info": "Lots 1 -47"
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