{
  "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": [
    {
      "status": "Terminated",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78835",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US, Germany, Sweden, Italy, Belgium, Portugal, Spain, France,  Russia, Poland, Turkey, China, Thailand, Taiwan, Hong Kong, Malaysia, Korea, and Mexico.",
      "recall_number": "Z-0411-2018",
      "product_description": "MARS Treatment Kit, Use only with MARS(R) Monitor 1TC, GAMBRO, Product Code 800541",
      "product_quantity": "186 units",
      "reason_for_recall": "Baxter has received customer complaints regarding leakage in the albumin circuit. The leakage was caused by an inadequate adhesive connection of the tubing to the Hansen connector of the MARS Tube Set which is part of the MARS Treatment Kit.",
      "recall_initiation_date": "20171221",
      "center_classification_date": "20180124",
      "termination_date": "20200804",
      "report_date": "20180131",
      "code_info": "UDI:  37332414107728; Lot Numbers:  0000022597, 0000022648, 0000022663, 0000022671, 0000022721, 0000022767"
    }
  ]
}