{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Danvers",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93581",
      "recalling_firm": "Abiomed, Inc.",
      "address_1": "24 Cherry Hill Dr",
      "address_2": "N/A",
      "postal_code": "01923-2575",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution nationwide.",
      "recall_number": "Z-0636-2024",
      "product_description": "Impella Connect, software portal for online device management that allows clinicians and Impella support staff to remotely view Impella data.",
      "product_quantity": "n/a - no physical product",
      "reason_for_recall": "The following features have been disabled from the web-based portal because the FDA has not evaluated these features for safety and effectiveness:    Notifications via email feature; AIC alarm color on case tile feature; Sort case tiles by AIC alarm color feature; Pump metric display on case tile feature",
      "recall_initiation_date": "20231206",
      "center_classification_date": "20240104",
      "report_date": "20240110",
      "code_info": "UDI-DI 00813502011647 Software version 1.1 - 3.17.1"
    }
  ]
}