{
  "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": [
    {
      "country": "United States",
      "city": "Waltham",
      "address_1": "920 Winter St",
      "reason_for_recall": "Dialysate Port Leak During Priming of the Dialyzers",
      "address_2": "",
      "product_quantity": "317,796 units",
      "code_info": "Lot Numbers:  13LU04022  13LU04021  13NU04003  13NU04005  13NU04018  13SU04002",
      "center_classification_date": "20140226",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) and the country of: Mexico.",
      "state": "MA",
      "product_description": "Optiflux F200NRe High Flux Dialyzers; Product Number: 0500320E.    Single Use acute or chronic hemanalysis treatment.",
      "report_date": "20140305",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Fresenius Medical Care Holdings, Inc.",
      "recall_number": "Z-1102-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67313",
      "termination_date": "20210518",
      "more_code_info": "",
      "recall_initiation_date": "20140204",
      "postal_code": "02451-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}