{
  "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": "31080",
      "product_res_number": "Z-0376-04",
      "event_date_initiated": "2003-12-17",
      "event_date_posted": "2004-01-29",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-11-28",
      "res_event_number": "28037",
      "product_code": "FRN--",
      "k_numbers": [
        "K002679"
      ],
      "product_description": "Baxter 6060 Multi-Therapy Infusion Pump, product code 2M9832; Manufactured by an affiliate of Baxter Healthcare Corp., Deerfield, IL 60013 USA, made in Singapore",
      "code_info": "serial numbers 108050HR, 108183HR, 108298HR, 109036HR, 109216HR, 109622HR, 110004HR, 110700HR, 111126HR, 111270HR, 111540HR, 112441HR, 201178HR, 308361HR/308440HR, 309001HJ/309030HJ, 309001HR/309345HR  309001HW/309015HW,  310001HG/310010HG , 310001HW/310010HW , 310007HR/310088HR, and HR1976/HR27480.  Only those pumps within these serial numbers with installed motor assemblies from date codes 33/03, 34/03 and 35/03 are affected.",
      "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": "Premature motor failure.",
      "root_cause_description": "Other",
      "action": "Baxter sent letters dated 12/17/03 to all Baxter 6060 Multi-Therapy Infusion Pump accounts that received pumps manufactured with the affected motors or who had their pumps refurbished with affected motors.  The letters included a list of affected pump serial numbers for each facility.  The accounts were informed of the possible premature motor failure, and were requested to contact Baxter via fax to schedule a service call to correct the pumps.",
      "product_quantity": "188 units",
      "distribution_pattern": "The product was distributed nationwide, and internationally to Sweden, Germany, the United Kingdom, Australia and Japan.",
      "openfda": {}
    }
  ]
}