{
  "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": "Labeling error.  Some shipping cartons labeled as ASK-04018-VUH contained ASK-04020-VUH kits; and some shipping cartons labeled as ASK-04020-VUH contained ASK-04018-VUH kits.",
      "address_2": "",
      "product_quantity": "50 units in total",
      "code_info": "Lot/Batch Numbers: 23F14M0829, 23F14M0986",
      "center_classification_date": "20160712",
      "distribution_pattern": "US distribution in the states of TN and KY.",
      "state": "PA",
      "product_description": "Femoral Arterial Line  Catheterization Kit with Sharps Safety Features  510K 810675, product code DQX, Device Listing D025180  Material ASK-04018-VUH    Product Usage:  The Arrow arterial catheterization device permits access to the peripheral arterial circulation.",
      "report_date": "20160720",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-2202-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74489",
      "termination_date": "20170821",
      "more_code_info": "",
      "recall_initiation_date": "20160602",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}