{
  "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": "2026-08-22",
    "results": {
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  "results": [
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      "cfres_id": "50038",
      "product_res_number": "Z-0574-2007",
      "event_date_initiated": "2007-01-08",
      "event_date_posted": "2007-03-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-02-07",
      "res_event_number": "37170",
      "product_code": "DSQ",
      "product_description": "AB5000 Console Circulatory Support System\nCatalog Number: 0015-0000",
      "code_info": "Serial Numbers: 5261- 5317",
      "firm_fei_number": "1220648",
      "recalling_firm": "Abiomed, Inc.",
      "address_1": "22 Cherry Hill Dr",
      "city": "Danvers",
      "state": "MA",
      "postal_code": "01923-2575",
      "additional_info_contact": "William Bolt\n978-777-5410",
      "reason_for_recall": "Unit may alarm ''Low Flow'' and ''Low Pressure'' due to manufacturing material in the pressure source.",
      "root_cause_description": "Other",
      "action": "Abiomed notified customers by letter dated 1/08/07. Service reps will inspect units and replace the defective components.",
      "product_quantity": "55 units",
      "distribution_pattern": "Worldwide, including USA, Japan, Germany, Australia, and Mexico.",
      "openfda": {
        "device_name": "Ventricular (Assist) Bypass",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3",
        "pma_number": [
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