{
  "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": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Potential leak in the balloon extension line. If a leak was present and went undetected during pre-use testing as outlined in the IFU, this would cause the balloon to deflate slowly following placement. If the leak went undetected by  attending clinicians during use, it could result in contrast injection into the vascular or cardiac tissue which could result in serious injury or death",
      "address_2": "",
      "product_quantity": "71 units",
      "code_info": "Lot Number: 16F19H0089",
      "center_classification_date": "20191219",
      "distribution_pattern": "U.S. Nationwide, Canada",
      "state": "PA",
      "product_description": "Arrow Berman Angiographic Catheter 50cc  Item Number:  AI-07130",
      "report_date": "20191225",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-0715-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84399",
      "termination_date": "20200619",
      "more_code_info": "",
      "recall_initiation_date": "20191115",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}