{
  "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": "Waukesha",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75851",
      "recalling_firm": "GE Healthcare, LLC",
      "address_1": "3000 N Grandview Blvd",
      "address_2": "N/A",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US:  AL, AR, AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT,NC, NE NH, NJ, NM, NY, NV, OH, OK, PA, RI, SC, SD, TN, TX,, VA, WA, WO, WY, WV.     OUS:     Algeria  Armenia  Australia  Austria  Brazil  Canada  Chile  China  Denmark  Egypt  France  Germany  Guatemala  Honduras  Hong Kong  Hungary  Iceland  India  Ireland  Italy  Japan  Korea  Libya  Mexico  Netherlands  Netherlands  Peru  Poland  Portugal  Russia  Saudi Arabia  Serbia  Sierra Leone  Slovakia  Spain  Taiwan  Thailand  Turkey  United Arab Emirates  United Kingdom  Venezuela  Vietnam",
      "recall_number": "Z-0910-2017",
      "product_description": "Precision 500D",
      "product_quantity": "Total for all products 1,598 (USA 824, OUS 774)",
      "reason_for_recall": "GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.",
      "recall_initiation_date": "20161121",
      "center_classification_date": "20161223",
      "termination_date": "20170926",
      "report_date": "20170104",
      "code_info": "Mfg. Lot or Serial # System ID  00000034206YY3 229353TR2  00000146304MO1 423778ERM4  Not Available 817255NHPD1"
    }
  ]
}