{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Pittsburgh",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85322",
      "recalling_firm": "Cardiac Assist, Inc",
      "address_1": "240 Alpha Dr",
      "address_2": "N/A",
      "postal_code": "15238-2906",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distributions.",
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      "product_description": "TandemHeart pump is assembled into kits:  TandemLife Kit  Product:  5740-0000 - Product Usage:  provides temporary extracorporeal circulatory system support with the unique ability to locally deliver an anticoagulant through the infusion system.",
      "product_quantity": "13",
      "reason_for_recall": "Failure to prime due to an assembly error",
      "recall_initiation_date": "20200306",
      "center_classification_date": "20200511",
      "termination_date": "20201120",
      "report_date": "20200520",
      "code_info": "Serial Numbers:  00142463  00142464  00142465  00142469  00142470  00142471  00142472  00142478  00142479  00142480  00142481  00142482  00142483"
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}