{
  "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": "100,008 units",
      "code_info": "Lot Numbers:  13LU02011  13LU02013  13NU02016  13NU02017",
      "center_classification_date": "20140226",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) and the country of: Mexico.",
      "state": "MA",
      "product_description": "Optiflux B200 Flux Dialyzers; Product Number: 0500325E.    Single Use acute or chronic hemanalysis treatment.",
      "report_date": "20140305",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Fresenius Medical Care Holdings, Inc.",
      "recall_number": "Z-1105-2014",
      "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"
    }
  ]
}