{
  "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": "Completed",
      "city": "Farmers Branch",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88317",
      "recalling_firm": "Epimed International",
      "address_1": "13958 Diplomat Dr",
      "address_2": "N/A",
      "postal_code": "75234-8805",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution, with US distribution to CA, DE, OH, OK, PA, VA, WA, WV.  International distribution to Canada and Iran.",
      "recall_number": "Z-2312-2021",
      "product_description": "NEO-KATH Epidural Catheter Set, REF 200-2430, Sterile",
      "product_quantity": "132 units",
      "reason_for_recall": "Potential for stylet to protrude from the distal end of the catheter",
      "recall_initiation_date": "20171228",
      "center_classification_date": "20210818",
      "report_date": "20210825",
      "code_info": "Reference Number 200-2430, Lot Numbers 16308275 (Expiration August 2022), 16308382 (Expiration October 2022)"
    }
  ]
}