{
  "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": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82984",
      "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 Nationwide Distribution",
      "recall_number": "Z-0053-2020",
      "product_description": "Pediatric Two-Lumen Central Venous Catheterization  Kit with Blue FlexTip ARROWg+ard Blue Catheter, REF AK-25502    Product Usage;  Provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access",
      "product_quantity": "3,143",
      "reason_for_recall": "Lidstock contains a labeling error.  The lidstock shows the catheter cross section of the gauge (GA) values in a reversed manner.",
      "recall_initiation_date": "20190517",
      "center_classification_date": "20191007",
      "termination_date": "20200924",
      "report_date": "20191016",
      "code_info": "Lot/Batch Numbers:  13F18C0374, 13F18H0580, 13F18D0504, 13F18L0507,   13F18E0380, 13F18L0714, 13F18G0180, 13F18L0936,   13F18G0480"
    }
  ]
}