{
  "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:  2C1008KP, 2C1009KP, 2C1063KP, 2C1087KP, 2C1156KP, 2C1700KP, 2C1702KP    Lot Codes:  10F032  10G056  10H066  10J047  10K024  10K087  10M021  10M088  10F059  10F069  10F070  10G029  10G043  10G062  10G067  10H032  10H093  10J049  10J060  10J089  10J105  10K028  10K030  10K038  10K088  10K096  10K102  10M025  10M044  10F022  10F068  10F072  10G030  10G045  10G046  10G047  10G050  10G051  10H016  10H018  10H087  10H094  10J053  10J058  10J062  10J102  10K026  10K035  10K039  10K086  10M023  10M040  10M043  10M045  10F020  10F087  10H086  10H095  10J017  10J020  10J056  10J068  10K021  10K029  10K031  10K081  10K105  10M017  10M039  10J052  10K098  10F064  10H044  10K022  10K042  10F024  10F025  10F033  10F055  10F062  10F063  10F065  10H005  10H030  10H042  10J015  10J019  10J061  10J065  10K032  10K037  10K095  10M030  10M087  10M098  10M099  10M100    Expiration Date: 06/30/13",
      "center_classification_date": "20130627",
      "distribution_pattern": "Distributed Nationwide and in Puerto Rico.",
      "state": "IL",
      "product_description": "Brand Name: Infusor SV and LV Elastomeric Infusion Devices.    Indicated for the intravenous administration of medications.",
      "report_date": "20130703",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Baxter Healthcare Corp.",
      "recall_number": "Z-1600-2013",
      "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"
    }
  ]
}