{
  "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": "Danvers",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93876",
      "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": "US Nationwide distribution.",
      "recall_number": "Z-1175-2024",
      "product_description": "Automated Impella Controller (AIC), Product No. 0042-0000-US, 0042-0010-US, 0042-0040-US.  Used with Impella Ventricular Support Systems (cardiovascular)",
      "product_quantity": "4,463 (US)",
      "reason_for_recall": "Retrospective reporting for the release of Technical Bulletin IMP-2643 AIC Version 8.5 Software Update Available. The update resolved an issue in version 8.4 where a pump was not recognized by the AIC.",
      "recall_initiation_date": "20210301",
      "center_classification_date": "20240222",
      "termination_date": "20250306",
      "report_date": "20240228",
      "code_info": "Product Code 0042-0000-US UDI-DI 00813502010022; Product Code 0042-0010-US UDI-DI 00813502010985; Product Code 0042-0040-US UDI-DI 00813502011401;  Software Versions V8.4 and V8.4.1"
    }
  ]
}