{
  "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": "2026-09-09",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Waltham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99543",
      "recalling_firm": "Fresenius Medical Care Renal Therapies Group, LLC",
      "address_1": "920 Winter St Bld 920",
      "address_2": "N/A",
      "postal_code": "02451-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the country of Mexico.",
      "recall_number": "Z-3091-2026",
      "product_description": "GRANUFLO Dry Acid Concentrate:  Product Numbers:  0FD2251-3B; 0FD3251-3B; Dry Acid Concentrate for Bicarbonate Hemodialysis",
      "product_quantity": "27,216 cs; 2,316 ea",
      "reason_for_recall": "Complaints of blue-green discoloration in product",
      "recall_initiation_date": "20260714",
      "center_classification_date": "20260903",
      "report_date": "20260909",
      "code_info": "1) 0FD2251-3B, UDI/DI 00840861101535, Lot Numbers:  26AXGF015, 26AXGF016, 26AXGF017, 26BXGF008, 26BXGF009;  2) 0FD3251-3B, UDI/DI 00840861101597, Lot Numbers:  26AXGF014, 26AXGF018.",
      "more_code_info": ""
    }
  ]
}