{
  "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": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Certain lots of peripheral catheter systems may be missing the safety latch, intended to minimize the risk of sharps injuries.",
      "address_2": "",
      "product_quantity": "305",
      "code_info": "Catalog Number: EDC-00820, Lot: 14X17C0039 (Expires February 2019); Catalog Number: EDC-00820-B, Lot: 13F17F0120 (Expires May 2019)",
      "center_classification_date": "20180326",
      "distribution_pattern": "Distributed in the following U.S. states: CO, FL, IL, NC, PA, SC, and TX.",
      "state": "PA",
      "product_description": "ARROW ENDURANCE\" Extended Dwell Peripheral Catheter System, Catalog Numbers: EDC-00820 & EDC-00820-B",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-1194-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79474",
      "termination_date": "20190718",
      "more_code_info": "",
      "recall_initiation_date": "20171215",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}