{
  "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": "Bothell",
      "address_1": "22100 Bothell Everett Hwy",
      "reason_for_recall": "A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound System.  The system will report incorrect Doppler velocities if you use High Pulse Repetition Frequency (HPRF) with multiple sample volume gates. While in High Pulse Repetition Frequency (HPRF) in \u0018Display Zoom  Velocity Scale\u0019 using manual spectral Doppler trace, the velocities in the velocity results table may be overstated b",
      "address_2": "",
      "product_quantity": "1267 total :670 units in US and 1267 units Internationally (which includes 11 units in Canada)",
      "code_info": "All systems below software v1.1.2 Which includes software v1 and  v 1.1 (All lot codes shipped prior to 2/28/2014).",
      "center_classification_date": "20140320",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) including states of: AL, AK, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NM, NJ, NM, NY, OH, OK, PA, SC, TN, TX, VA, WA, and WV; and countries of: Australia, Austria, Belgium, Canada, Chili, Ecuador, Egypt, Finland, France, Germany, Greece, India, Ireland, Italy, Japan, Korea Rep, Malaysia, Netherlands, New Zealand, Norway, Peru, Philippines, Portugal, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Switzerland, Thailand, Turkey and United Kingdom.",
      "state": "WA",
      "product_description": "Philips Model EPIQ 7 Ultrasound System.  Intended for diagnostic ultrasound imaging and fluid flow analysis.    Catalogue numbers 795200 / 795201 / 795202 / 795204 / 795205 / 795206    EPIQ is intended for diagnostic ultrasound imaging and fluid flow analysis. The collection of Doppler velocity results values are used to assist in diagnosing the existence, location and severity of cardiac or vasculare stenosis.",
      "report_date": "20140326",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Medical Systems North America Inc.",
      "recall_number": "Z-1264-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67685",
      "termination_date": "20161212",
      "more_code_info": "",
      "recall_initiation_date": "20140228",
      "postal_code": "98021-8431",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}