{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Danvers",
      "state": "MA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98276",
      "recalling_firm": "Abiomed, Inc.",
      "address_1": "22 Cherry Hill Dr",
      "address_2": "N/A",
      "postal_code": "01923-2575",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide  and the countries of Austria, Canada, Croatia, Czechia, France, Germany, Hong Kong, Italy, Poland, Serbia, Switzerland.",
      "recall_number": "Z-1470-2026",
      "product_description": "Impella RP Flex with SmartAssist. Product Code: 1000323.",
      "product_quantity": "4,496 units",
      "reason_for_recall": "Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.",
      "recall_initiation_date": "20260127",
      "center_classification_date": "20260227",
      "report_date": "20260311",
      "code_info": "Product Code: 1000323. UDI-DI: 00813502012811."
    }
  ]
}