{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "43484",
      "product_res_number": "Z-0656-06",
      "event_date_initiated": "2005-12-15",
      "event_date_posted": "2006-03-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-08-18",
      "res_event_number": "34290",
      "product_code": "FMG",
      "k_numbers": [
        "K022895",
        "K921899",
        "K962581",
        "K984381"
      ],
      "product_description": "Baxter Interlink System Buretrol Solution Set with Large Bore 4-Way Stopcock with Rotating Male Luer Lock Extension Set and  Extension Set, product code 3C0172; An Rx sterile, nonpyrogenic fluid pathway; solution set: 84'', 60 drops/mL, with 150 mL Burette Drip Chamber Filter Valve, 3 injection sites and male Luer Lock adapter, stopcock extension set: 21'', 3.2 mL Vol with 2 injection sites and male luer adapter, and minivolume extension set: 6'', 0.5 mL Vol with microvolume tubing and retractable T-connector; Baxter Healthcare Corporation, Deerfield, IL 60015 U.S.A.",
      "code_info": "product code 3C0172, lot GR230631",
      "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": "Center for One Baxter\n800-422-9837",
      "reason_for_recall": "The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.",
      "root_cause_description": "Other",
      "action": "Baxter sent Urgent Product Recall letters dated 8/3/05 to their customers, to the attention of the Director of Materials Management, via first class mail on the same date. The accounts were informed of the microbore female luers that may crack during use, resulting in the possible under delivery or incomplete delivery of medication. The accounts were instructed to examine their inventory for the affected lots of product, remove it from inventory and return it to Baxter for credit. Any questions were directed to the Center for One Baxter at 1-800-422-9837. Baxter extended the recall to include additional lots and product codes via letter dated 12/15/05. The letters referenced the 8/3/05 letter, including a copy of that letter, and listed the affected lots of sets. The instructions for return of the product remained the same as that described in the 8/3/05 letter.",
      "product_quantity": "870 sets",
      "distribution_pattern": "Nationwide, including Puerto Rico and American Samoa, and internationally to Canada, Australia, Japan, South Korea, Saudi Arabia, India, Mexico, Venezuela, Malaysia, East Timor and New Zealand.",
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        "device_name": "Stopcock, I.V. Set",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5440",
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}