{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Johnstown",
      "address_1": "141 Sal Landrio Dr",
      "reason_for_recall": "Mislabeled - The product's labeling contains an incorrect size for the catheter included in the kit.  The kit contains a 21 gauge catheter, however the labeling states a 12 gauge catheter is included.",
      "address_2": "Crossroads Business Park",
      "product_quantity": "200 kits",
      "code_info": "Lot 31129155,  Exp: 2022-12-31",
      "center_classification_date": "20190724",
      "distribution_pattern": "Distribution in US states of CA, FL, OK, AR, WA, TX, ID, NY, South Africa, and Mexico",
      "state": "NY",
      "product_description": "Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED,  REF 181-2112, RX,  (01) 108187880213945, LOT 311291155   for  epidural or caudal anesthesia",
      "report_date": "20190731",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Epimed International, Inc.",
      "recall_number": "Z-2068-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83247",
      "recall_initiation_date": "20190618",
      "postal_code": "12095-3835",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}