{
  "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": "Farmers Branch",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77842",
      "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": "Domestic: AR, CA, IA, IN, KY, LA, MI, NY, OH, OR, TN, TX, & WA. Foreign: Canada, Czech Republic, Germany ,& Turkey.",
      "recall_number": "Z-0087-2018",
      "product_description": "RX-2 COUDE Epidural Needle, 16g x 3.5in (8.9cm)TW, 10 units, Calibrated, Plastic Hub, Detachable Wing, Blunt Stylet, Sterile, Rx only, For Use with 19g or Smaller Catheter",
      "product_quantity": "500 units",
      "reason_for_recall": "Potential for partially incomplete seal of product, impacting sterility.",
      "recall_initiation_date": "20170724",
      "center_classification_date": "20171109",
      "termination_date": "20230706",
      "report_date": "20171115",
      "code_info": "Lot No. 12168200; Ref No. 107-1416."
    }
  ]
}