{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90841",
      "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 Nationwide",
      "recall_number": "Z-0082-2023",
      "product_description": "Prismaflex M Set:  M150 (product code 109990).  For use in providing continuous fluid management and renal replacement therapies.",
      "product_quantity": "334,932 devices",
      "reason_for_recall": "Within the current Prismaflex set IFU (instructions for use), there is a mistranslation of the Extonian (Eesti) text.  The mistranslation indicates contradictory information related to the patient body weight restrictions.",
      "recall_initiation_date": "20220914",
      "center_classification_date": "20221012",
      "report_date": "20221019",
      "code_info": "UDI 07332414090005; All Lot Codes"
    }
  ]
}