{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "48062",
      "product_res_number": "Z-0015-2007",
      "event_date_initiated": "2004-01-26",
      "event_date_posted": "2006-10-04",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-11-27",
      "res_event_number": "36138",
      "product_code": "DSQ",
      "pma_numbers": [
        "P920014",
        "P870072"
      ],
      "product_description": "Thoratec brand Sealed Arterial Cannula for use with the Thoratec Vascular Assist Device System, \nModel Number(s): Catalogue numbers: \n\t#100118-- Short, 14mm graft;\n\t#100121-- Long, 14mm graft;\n\t#100129-- Long, 18mm graft.\nManufactured by Thoratec Corporation, 6035 Stoneridge Drive, Pleasanton, CA 94588",
      "code_info": "Serial Numbers: 104, 106",
      "firm_fei_number": "2916596",
      "recalling_firm": "Thoratec  Corp",
      "address_1": "6035 Stoneridge Drive",
      "city": "Pleasanton",
      "state": "CA",
      "postal_code": "94588-3270",
      "additional_info_contact": "Donald A. Middlebrook\n925-730-4117",
      "reason_for_recall": "During use an unexpected flaking of the inner surface coating (blood contact) that has the potential for risk of embolism.",
      "root_cause_description": "Other",
      "action": "On 1/26/2004, the firm issued letters via Federal Express to all its direct consignees, informing them of the affected product and providing instructions on the recall.",
      "product_quantity": "11 units",
      "distribution_pattern": "Nationwide to 11(eleven) hospitals.  The product was shipped within the United States in IL, MA, NC, MD, MO, FL, CA, AZ, PA, and NY.  The product was distributed to one consignee in Australia.",
      "openfda": {
        "device_name": "Ventricular (Assist) Bypass",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3",
        "pma_number": [
          "P170038",
          "P980012",
          "P900023",
          "P870072",
          "P160035",
          "P160054",
          "P920014",
          "P060040",
          "P100047"
        ],
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          "1927395",
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}