{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Round Lake",
      "address_1": "Route 120 And Wilson Rd",
      "reason_for_recall": "Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for the products listed above due to an increase in rupture complaints.  Baxter has implemented product and process improvements which have substantially improved product quality. Complaint rates for ruptures have since decreased. Baxter wants to ensure that no affected product remains in the field.",
      "address_2": "",
      "product_quantity": "3,255,096 total",
      "code_info": "Product Codes:  2C1730K, 2C1732K, 2C1734K, 2C1740K, 2C1743K, 2C1744K    Lot Codes:  10F009  10F049  10F053  10F057  10F095  10J006  10J079  10K077  10M067  10F004  10F015  10G016  10G017  10G018  10G019  10G053  10G054  10H007  10H008  10H009  10H049  10H050  10H051  10H079  10H080  10H081  10H108  10J002  10J009  10J011  10J012  10J077  10J078  10J083  10K009  10K010  10K011  10K012  10K014  10K018  10K070  10K071  10K072  10M015  10M061  10M066  10M071  10M073  10M074  10M082  10F010  10F011  10F079  10G021  10G022  10G023  10H010  10H025  10H026  10H047  10J003  10J004  10J005  10J080  10J081  10J082  10J093  10K016  10K017  10K019  10M008  10M010  10M075  10M078  10M080  10M081  10H083  10M065  10F051  10F073  10G039  10G040  10J007  10J008  10J109  10K007  10K057  10K106  10M064  10M070  10F005  10F006  10F052  6/19/2010   6/22/2010   6/23/2010   8/13/2010   8/23/2010   8/30/2010   9/3/2010   9/30/2010   10/4/2010   10/21/2010   10/26/2010   11/4/2010   11/15/2010   11/24/2010     Expiration Date: 06/30/13",
      "center_classification_date": "20130627",
      "distribution_pattern": "Distributed Nationwide and in Puerto Rico.",
      "state": "IL",
      "product_description": "Brand Name: Intermate Infusion Pump.    Indicated for the intravenous administration of medications.",
      "report_date": "20130703",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Baxter Healthcare Corp.",
      "recall_number": "Z-1604-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65365",
      "termination_date": "20140604",
      "more_code_info": "",
      "recall_initiation_date": "20130607",
      "postal_code": "60073-9799",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}