{
  "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": "2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may fail to detect a disconnected Ultrafiltration (UF) Pump",
      "address_2": "",
      "product_quantity": "79 units",
      "code_info": "Revision K Actuator Test Boards  S/N of 2008 T Machines:  3T0S124903  3T0S124937  3T0S124933  3T0S124986  3T0S124934  3T0S124970  3T0S124894  3T0S124935  3T0S124912  3T0S124965  3T0S124944  3T0S124988  3T0S124939  3T0S124990  3T0S124940  3T0S124941  3T0S124958  3T0S124888  3T0S124946  3T0S124999  3T0S124942  3T0S124991  3T0S125023  3T0S124951  3T0S124936  3T0S124895  3T0S124955  3T0S125000  3T0S124943  3T0S125010  3T0S124893  3T0S124954  3T0S124896  3T0S124899  3T0S124959  3T0S125008  3T0S124947  3T0S125018  3T0S124905  3T0S124961  3T0S124898  3T0S124907  3T0S124963  3T0S124891  3T0S124952  3T0S125028  3T0S124920  3T0S124966  3T0S124910  3T0S124909  3T0S124967  3T0S124901  3T0S124953  3T0S125029  3T0S124922  3T0S124969  3T0S124913  3T0S124911  3T0S124972  3T0S124902  3T0S124960  3T0S124930  3T0S124925  3T0S125011  3T0S124921  3T0S124916  3T0S124979  3T0S124918  3T0S124962  3T0S124945  3T0S124926  3T0S125013  3T0S124927  3T0S124917  3T0S124984  3T0S124928  3T0S124968  3T0S124964  3T0S124932",
      "center_classification_date": "20140513",
      "distribution_pattern": "USA (nationwide) and the country of Canada.*",
      "state": "MA",
      "product_description": "Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards and  also sold as replacement parts for use with Fresenius 2008-Series Hemodialysis Machines (2008K, 2008K2, 2008K@home and 2008T).     Part Number: 190234 Revision K",
      "report_date": "20140521",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Fresenius Medical Care Holdings, Inc.",
      "recall_number": "Z-1618-2014",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "68042",
      "termination_date": "20210518",
      "more_code_info": "",
      "recall_initiation_date": "20140425",
      "postal_code": "02451-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}