{
  "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": {
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  "results": [
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      "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",
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      "product_description": "TandemHeart Pump Kit, Product: 5120-0000 - Product Usage:  provides temporary extracorporeal circulatory system support with the unique ability to locally deliver an anticoagulant through the infusion system.",
      "product_quantity": "10",
      "reason_for_recall": "Failure to prime due to an assembly error",
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      "center_classification_date": "20200511",
      "termination_date": "20201120",
      "report_date": "20200520",
      "code_info": "Serial Numbers:  00142577  00142578  00142579  00142656  00142675  00142944  00142946  00142947  00142960  00142961"
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}