{
  "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": [
    {
      "country": "United States",
      "city": "Mansfield",
      "address_1": "120 Forbes Blvd Ste 170",
      "reason_for_recall": "A pump alarm function anomaly in the pump firmware code may result in the pump not sending the expected error code notifications to the Programmer, or not emit an audible alarm tone in certain \"out of tolerance\" conditions associated with the pump's valve system.",
      "address_2": "",
      "product_quantity": "1083 (OUS)",
      "code_info": "All units with pump firmware version 0.26 manufactured from 2012 until the present time.",
      "center_classification_date": "20200210",
      "distribution_pattern": "Nationwide domestic distribution. Foreign distribution to United Kingdom, Republic of Ireland, Poland, Greece, Italy, Germany, Netherlands, and Belgium.",
      "state": "MA",
      "product_description": "Prometra II Programmable 20mL Pump. Catalog No. 93827  The device is an implantable infusion pump. GTIN-14 00810335020YYY (YYY= in-country language specific)",
      "report_date": "20200219",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Flowonix Medical Inc",
      "recall_number": "Z-1125-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84653",
      "more_code_info": "",
      "recall_initiation_date": "20191224",
      "postal_code": "02048-1150",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}