{
  "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": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74898",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "address_2": "N/A",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states of: NC, OH, FL, and MD.",
      "recall_number": "Z-2773-2016",
      "product_description": "Catheter, Percutaneous    The Arrow Single-Lumen Catheter permits venous access to the central circulation.",
      "product_quantity": "6,121 units in total",
      "reason_for_recall": "Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products.",
      "recall_initiation_date": "20160217",
      "center_classification_date": "20160909",
      "termination_date": "20171018",
      "report_date": "20160921",
      "code_info": "Lot/Batch Numbers:   23F15L0662,23F15J0260,23F15K0983,23F15G0159,23F15J1102,23F15J0259  23F15C1225,23S15G0973,23F15H1033,23F15F0358,23F15K0345,23F15D1514  23F15C1226,23F15H0919,23F15E1091,23F15H0014,23F15D0241,23F15J0533  23F15E1094,23F15H0020,23F15H0740,23F15K1009,23F15J0431,23F15F1836  23F15H0857,23F15K0012,23F15M0313,23F15G0871,23F15J0285",
      "more_code_info": ""
    }
  ]
}