{
  "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": "Terminated",
      "city": "Johnstown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87333",
      "recalling_firm": "Epimed International, Inc.",
      "address_1": "141 Sal Landrio Dr",
      "address_2": "N/A",
      "postal_code": "12095-3835",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution",
      "recall_number": "Z-1276-2021",
      "product_description": "Feth-R-Kath Catheter, 19g x 24\". Intended Use:Radlo Opaque Epidural Catheter  Catalog #: 157-1924     Intended for epidural anesthesia and is limited to placement of 72 hours or less",
      "product_quantity": "5835 units",
      "reason_for_recall": "Outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off",
      "recall_initiation_date": "20210201",
      "center_classification_date": "20210318",
      "termination_date": "20221017",
      "report_date": "20210324",
      "code_info": "Lot Numbers: 11247915, 11248510, 11248553, 11248938, 11248985, 11249049"
    }
  ]
}