{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Louis",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72710",
      "recalling_firm": "Partners In Medicine Llc",
      "address_1": "11469 Olive Blvd Ste 127",
      "address_2": "N/A",
      "postal_code": "63141-7108",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide Distribution including MI and CA.",
      "recall_number": "Z-0572-2016",
      "product_description": "CNSystems TASK FORCE MONITOR 3040i, plethysmograph, impedance.  Noninvasively measure and display patient's hemodynamic parameters time synchronized using Impedance Cardiography (ICG), Electrocardiography (ECG), oscillometric Blood Pressure (oscBP) and continuous Blood Pressure (contBP). Furthermore Sympathic Tone and Parasympathic Tone are calculated by power spectral analysis of ECG (heart rate variability) and continuous blood pressure (blood pressure variability) as well as the Baroreceptor Reflex Sensitivity (BRRS). For use by medically trained personnel. It has been designed for diagnoses aiding and must not be used for vital sign monitoring of critically ill patients under absence of additional, suitable self-monitoring devices or medical trained personnel. The device measures continuously the subject's hemodynamic parameters without reporting any diagnosis. It is the physician's responsibility to make proper judgment based on these parameters.",
      "product_quantity": "28 worldwide 2 monitors distributed in the U.S.",
      "reason_for_recall": "Device non-conformity which may lead to an incorrect oscillometric measurement of upper arm blood pressure values in some subjects - mainly in tall and slim persons (overestimation of systolic blood pressure, underestimation of diastolic blood pressure).",
      "recall_initiation_date": "20151201",
      "center_classification_date": "20160104",
      "termination_date": "20170217",
      "report_date": "20160113",
      "code_info": "Serial numbers:  003040i-2014-161-014-GG-0000,  003040i-2015-101-003-GG-0000,  003040i-2014-161-001-GG-0000,  003040i-2014-161-002-GG-0000,  003040i-2014-161-003-GG-0000,  003040i-2014-161-004-GG-0000,  003040i-2014-161-005-GG-0000,  003040i-2014-161-006-GG-0000,  003040i-2014-161-007-GG-0000,  003040i-2014-161-008-GG-0000,  003040i-2014-161-009-GG-0000,  003040i-2014-161-010-GG-0000,  003040i-2014-161-011-GG-0000,  003040i-2014-161-012-GG-0000,  003040i-2014-161-013-GG-0000,  003040i-2014-161-015-GG-0000,  003040i-2014-161-016-GG-0000,  003040i-2014-161-017-GG-0000,  003040i-2014-161-018-GG-0000,  003040i-2014-161-019-GG-0000,  003040i-2014-161-020-GG-0000,  003040i-2014-161-021-GG-0000,  003040i-2014-161-022-GG-0000,  003040i-2014-161-023-GG-0000,  003040i-2014-161-024-GG-0000,  003040i-2014-161-025-GG-0000,  003040i-2015-101-001-GG-0000, and  003040i-2015-101-002-GG-0000"
    }
  ]
}