{
  "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": "2026-04-01",
    "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": "88351",
      "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 distribution.",
      "recall_number": "Z-2379-2021",
      "product_description": "Baxter prismaflex, HF 1000 PAES membrane, REF 107140     Used with Prismaflex or PrisMax control units for continuous fluid management and renal replacement therapies.",
      "product_quantity": "1976 units",
      "reason_for_recall": "Products labeled as sterile were distributed, but may not have been sterilized.  Baxter confirmed Steril Milano observed nonconformances that were not reported to Baxter  Data was manipulated to appear to be conforming",
      "recall_initiation_date": "20210722",
      "center_classification_date": "20210827",
      "termination_date": "20240117",
      "report_date": "20210908",
      "code_info": "Lot Numbers:  20B2330M"
    }
  ]
}