{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "36005",
      "product_res_number": "Z-0301-05",
      "event_date_initiated": "2004-11-05",
      "event_date_posted": "2004-12-09",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-05-16",
      "res_event_number": "30495",
      "product_code": "KDJ",
      "k_numbers": [
        "K883239"
      ],
      "product_description": "Baxter CAPD Solution Transfer Set for use with UV-Flash Germicidal Exchange Device, 1.2 m (48''); a sterile set consisting of a bag connector (spike connector), on-off clamp assembly, tubing and double sealing male Luer lock connector; Baxter Healthcare Corporation, Renal Division, McGaw Park, IL 60085; product code R5C4325",
      "code_info": "Product code R5C4325, lot H03L12057, expiration date 12/31/08",
      "firm_fei_number": "3000210122",
      "recalling_firm": "Baxter Healthcare Renal Div",
      "address_1": "1620 Waukegan Rd Bldg R Mc Gaw",
      "city": "Park",
      "state": "IL",
      "postal_code": "60085-6730",
      "additional_info_contact": "Center for One Baxter\n800-422-9837",
      "reason_for_recall": "Disconnection of the tubing at the clamp level of the UV Flash Transfer Set.",
      "root_cause_description": "Other",
      "action": "Recall by letter dated 11/05/04.  The customers were instructed to stop using this lot of product, return any stocks of the lot back to Baxter, and that replacement of the patient''s set be completed at the dialysis center.",
      "product_quantity": "1,152 sets",
      "distribution_pattern": "The entire lot was distributed overseas to Belgium, Sweden, Norway, the United Kingdom, Germany and France.",
      "openfda": {
        "k_number": [
          "K801193",
          "K945567",
          "K780957",
          "K963668",
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          "K895991",
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          "K921818",
          "K792651",
          "K900226",
          "K904806",
          "K851207",
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          "K083542",
          "K810671",
          "K900323",
          "K900142",
          "K895990",
          "K791722",
          "K900012",
          "K151620",
          "K883393",
          "K771482",
          "K892870",
          "K896763",
          "K900242",
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          "K781755",
          "K152129",
          "K900004",
          "K812771",
          "K214016",
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          "K921052",
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          "K870145",
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          "K810600",
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          "K852678",
          "K871050",
          "K173651",
          "K893231",
          "K972731",
          "K896599"
        ],
        "device_name": "Set, Administration, For Peritoneal Dialysis, Disposable",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.5630",
        "device_class": "2",
        "registration_number": [
          "3013188547",
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        ],
        "fei_number": [
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          "1000219637",
          "3002807005",
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}