{
  "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.",
      "recall_number": "Z-1950-2020",
      "product_description": "TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A17, Product:  5710-6217 - Product Usage:  provides temporary extracorporeal circulatory system support with the unique ability to locally deliver an anticoagulant through the infusion system.",
      "product_quantity": "15",
      "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:  S/N  00142612  00142614  00142657  00142658  00142659  00142660  00142661  00142663  00142937  00142938  00142941  00142942  00142970  00142971  00142972"
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}