{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 89
    }
  },
  "results": [
    {
      "cfres_id": "40930",
      "product_res_number": "Z-0174-06",
      "event_date_initiated": "2005-07-22",
      "event_date_posted": "2005-11-23",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-05-24",
      "res_event_number": "32844",
      "product_code": "CAC",
      "k_numbers": [
        "K043127"
      ],
      "product_description": "cardioPAT Cardiovascular Perioperative Autotransfusion System, Model: LN 2050-110-E\nand Disposables:\ncardioPAT Replacement RBC Bags, LN 00270\ncardioPAT Replacement  Waste Bags, LN 00271\ncardioPAT Replacement  Intraoperative Suction Set, LN 00272\ncardioPAT Replacement  Postoperative Suction Set, LN 00273\ncardioPAT cardiovascular Perioperative Autotransfusion System Disposable Set, LN 00274\ncardioPAT Replacement One-Way Valve Assembly LN 00275",
      "code_info": "All lot numbers",
      "firm_fei_number": "1219343",
      "recalling_firm": "Haemonetics Corporation",
      "address_1": "400 Wood Rd",
      "city": "Braintree",
      "state": "MA",
      "postal_code": "02184-2412",
      "additional_info_contact": "781-356-9488",
      "reason_for_recall": "Blood clotting of patient post operative while on the cardioPAT Cardiovascular Perioperative Autotransfusion  System",
      "root_cause_description": "Other",
      "action": "Haemonetics issued a recall notification via Certified Mail on 7/22/05 to four user sites requesting return of the machine and all disposables received.",
      "product_quantity": "4 machines and 486 disposables",
      "distribution_pattern": "CA, MN, NE, TX",
      "openfda": {
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        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.5830",
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}