{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Palm Harbor",
      "address_1": "612 Florida Ave",
      "reason_for_recall": "On 07/09/2012, Apheresis Technologies, Inc. initiated a recall on the Plasma Pump Model PP-04a due to a complaint received regarding a rotor of the PP-04a pump that stopped during a therapeutic plasma exchange treatment causing interruption of flow of both the plasma discard line and replacement fruit line.",
      "address_2": "",
      "product_quantity": "13",
      "code_info": "D11003544 through D11003552  D11003556 through D11003558",
      "center_classification_date": "20120806",
      "distribution_pattern": "Natonwide Distribution",
      "state": "FL",
      "product_description": "Plasma Pump Model PP-04a    Used with Asahi Plasmaflo Plasma Separators and plasma exchange tubesets to perform therapeutic plasma exchange.",
      "report_date": "20120815",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Apheresis Technologies, Inc.",
      "recall_number": "Z-2149-2012",
      "initial_firm_notification": "Visit",
      "product_type": "Devices",
      "event_id": "62563",
      "termination_date": "20131216",
      "more_code_info": "",
      "recall_initiation_date": "20120709",
      "postal_code": "34683-5459",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}