{
  "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": "Ongoing",
      "city": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91021",
      "recalling_firm": "ARROW INTERNATIONAL Inc.",
      "address_1": "3015 Carrington Mill Blvd",
      "address_2": "N/A",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide",
      "recall_number": "Z-0430-2023",
      "product_description": "Arrow AutoCAT2 Intra-Aortic Balloon Pump,  AUTOCAT2 WAVE REFURBISHED, REF IAP-0500X (IPN000328),  cardiac pump",
      "product_quantity": "88 units",
      "reason_for_recall": "There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.",
      "recall_initiation_date": "20221017",
      "center_classification_date": "20221215",
      "report_date": "20221221",
      "code_info": "UDI/DI (01) 0 0801902 09391 2, (01) 0 0801902 09391 3, All Lot/Serial Numbers"
    }
  ]
}