{
  "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-1951-2020",
      "product_description": "TandemHeart pump is assembled into kits: ProtekDuo Kit - DL29, Product:  5720-2916 - Product Usage:  provides temporary extracorporeal circulatory system support with the unique ability to locally deliver an anticoagulant through the infusion system.",
      "product_quantity": "38",
      "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:  00142569  00142570  00142571  00142572  00142573  00142574  00142575  00142576  00142592  00142593  00142594  00142595  00142597  00142598  00142600  00142601  00142664  00142665  00142666  00142668  00142669  00142670  00142671  00142672  00142673  00142674  00142692  00142693  00142694  00142696  00142697  00142698  00142699  00142926  00142930  00142933  00142936  00142934"
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