{
  "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/",
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    "results": {
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      "state": "MA",
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      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
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      "recalling_firm": "Covidien Llc",
      "address_1": "15 Hampshire St",
      "address_2": "N/A",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "product_quantity": "278 total",
      "reason_for_recall": "Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.",
      "recall_initiation_date": "20211104",
      "center_classification_date": "20211209",
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      "report_date": "20211215",
      "code_info": "GTIN/UDI - 10884521174177  Serial Numbers: 35B1700627 35B1700628 35B1700629 35B1700630 35B1700631 35B1700632",
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}