{
  "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,
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  },
  "results": [
    {
      "cfres_id": "94561",
      "product_res_number": "Z-0356-2011",
      "event_date_initiated": "2010-09-17",
      "event_date_posted": "2010-11-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-10-04",
      "res_event_number": "56792",
      "product_code": "LBJ",
      "product_description": "Baxter CLEARLINK System, Non-DEHP Catheter Extension Set Kit; 8.2\" (21.0 cm), Vol. 0.57 mL, 1 Catheter Extension Set with luer activated valve for IV Access and male luer lock adapter, 1 VITAL-HOLD Medium Catheter Stabilization Device,  2 foam tape strips; an Rx sterile convenience kit for IV infusions; 50 units per case; Manufactured by an affiliate of Baxter Healthcare Corp., Deerfield, IL 60015 U.S.A., Made in Costa Rica; catalog 2N8222",
      "code_info": "catalog 2N8222, lot number R10B01028",
      "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 removable paper liner covering the adhesive strip that is used to secure the catheter stabilization device to the patient is pyrogenic. The device is labeled as nonpyrogenic.",
      "root_cause_description": "Component design/selection",
      "action": "Baxter issued Urgent Product Recall letters dated September 17, 2010 to the affected direct accounts. The accounts were informed that the paper lining covering the adhesive strip that is used to secure the catheter stabilization device to the patient was found to be pyrogenic. The accounts were requested to discontinue use and segregate the affected lots of products from inventory and call Baxter Healthcare Center for Service at 1-888-229-0001, Monday through Friday, 7:00 AM to 6:00 PM CT, to arrange for the return of the affected product for credit. The accounts were also requested to complete and fax back to Baxter the enclosed reply sheet confirming receipt of the letter and the amount of each product being returned. If the accounts further distributed the products, they were requested to forward the communication to those accounts. \nClinical questions regarding the communication are directed to the Medical Information Services at Baxter at 1-800-933-0303.  Any other questions may be directed to the Center for One Baxter at 1-800-422-9837.",
      "product_quantity": "11,800 units",
      "distribution_pattern": "Nationwide Distribution: Throughout the US.",
      "openfda": {
        "device_name": "Device, Vein Stabilization",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.6980",
        "device_class": "1",
        "registration_number": [
          "3006260740",
          "1018233",
          "3006082230",
          "1417592",
          "9617592"
        ],
        "fei_number": [
          "3006260740",
          "1018233",
          "3006082230",
          "3002468371",
          "1417592"
        ]
      }
    }
  ]
}