{
  "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": "Ongoing",
      "city": "Waltham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90438",
      "recalling_firm": "Fresenius Medical Care Holdings, Inc.",
      "address_1": "920 Winter St Bld 950",
      "address_2": "",
      "postal_code": "02451-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Natiowide",
      "recall_number": "Z-1371-2022",
      "product_description": "NATURALYTE Liquid Acid 3.0K 3.0Ca- indicated for use in patients undergoing extracorporeal bicarbonate hemodialysis for acute and chronic renal failure  Part Number: 08-3301-2",
      "product_quantity": "163 cases",
      "reason_for_recall": "Alternate Bottle Caps labeled with \"Sealed for your Protection\" on the foil not qualified for use",
      "recall_initiation_date": "20220531",
      "center_classification_date": "20220712",
      "report_date": "20220720",
      "code_info": "UDI-DI: (01) 10840861101757                (17) 240331                (10) 22CTAC102    Lot Number: 22CTAC102  Exp Date: 2024-03-31",
      "more_code_info": ""
    }
  ]
}