{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "25493",
      "product_res_number": "Z-0491-03",
      "event_date_initiated": "2002-12-16",
      "event_date_posted": "2003-01-30",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-08-21",
      "res_event_number": "25262",
      "product_code": "DSQ",
      "pma_numbers": [
        "P870072S012"
      ],
      "product_description": "Thoratec Sterile LVAD Pneumatic Lead 5'' ; \nModel/Product Number: 20010-0000-108",
      "code_info": "Lot Number: 17482",
      "firm_fei_number": "2916596",
      "recalling_firm": "Thoratec  Corp",
      "address_1": "6035 Stoneridge Drive",
      "city": "Pleasanton",
      "state": "CA",
      "postal_code": "94588",
      "reason_for_recall": "The product is mislabeled, in that the LVAD Pneumatic Lead 5' is identified with a BLUE Collar (instead of Red) in order to distinguish RVAD.",
      "root_cause_description": "Other",
      "action": "On 12/16/02, the firm initiated the recall and their notification was via letters requesting return of affected devices.",
      "product_quantity": "45 units",
      "distribution_pattern": "The unit containing the affected product was shipped to a total of 25 hospitals in IL, PA, NY, TX, WI, FL, IN, WA, OK, AL, and WA-DC.  The recall was appropriately extended to the consumer/user level; i.e., the hospitals, which received the recalled product.  There is no known U. S. Government accounts but there are 3 foreign accounts: Canada, France and Spain.",
      "openfda": {
        "device_name": "Ventricular (Assist) Bypass",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3",
        "pma_number": [
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          "P900023",
          "P170038",
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          "P160054",
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}