{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "25451",
      "product_res_number": "Z-0448-03",
      "event_date_initiated": "2002-12-18",
      "event_date_posted": "2003-01-16",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-09-30",
      "res_event_number": "25247",
      "product_code": "KSB",
      "k_numbers": [
        "K881321"
      ],
      "product_description": "Y-Type Blood/Solution Set, catalog #1C8029; Standard Blood Filter (170 to 260 micron), Drip Chamber Pump, Injection Site, Male Luer Lock Adapter, 111'' long, 10 drops per mL; Baxter Healthcare Corporation, Deerfield, IL 60015",
      "code_info": "lots GR182881, GR183558, GR184200, GR185900",
      "firm_fei_number": "1416980",
      "recalling_firm": "Baxter Healthcare Corp.",
      "address_1": "Rt 120 & Wilson Rd",
      "city": "Round Lake",
      "state": "IL",
      "postal_code": "60073",
      "additional_info_contact": "Cetenr for One Baxter\n800-422 Ext. 9837",
      "reason_for_recall": "Leakage may occur at the inlet port",
      "root_cause_description": "Other",
      "action": "The affected product codes and lot numbers were recalled by letter dated 12/18/02.  The customers were informed of the potential leakage at the inlet port, and were requested to inspect their inventory for the affected products and destroy those found.  The accounts were requested to complete the enclosed reply form and certificate of destruction and return them to Baxter for credit issuance.",
      "product_quantity": "21,134 sets",
      "distribution_pattern": "Nationwide",
      "openfda": {
        "k_number": [
          "K172957",
          "K791130",
          "K791131",
          "K820447",
          "K802940",
          "K001043"
        ],
        "registration_number": [
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        ],
        "device_name": "Set, Transfer (Blood/Plasma)",
        "medical_specialty_description": "Hematology",
        "regulation_number": "864.9875",
        "device_class": "2"
      }
    }
  ]
}