{
  "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-0906-2017",
      "product_description": "ADVANTX LCLP+",
      "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  00000047915YY4 415540ADVLCLP  00000063721YY5 909865LCLP  Not Available 916734XR  00000063736YY3 MCTHKGMN  00000023830YY3 912633MCL1  00000023761YY0 912633MCL1  00000128484M03 312CCHGECATH  00000128484MO3 312CCHGECATH  Not Available 507255CC101  Not Available LIJ015064  00000026160YY2 210428VCATH2  00000063805YY6 BPEP  Not Available 414C4862  00000022150YY7 YX0738"
    }
  ]
}