{
  "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": "70514",
      "recalling_firm": "GE Healthcare",
      "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": "Worldwide Distribution-US (nationwide) including the states of  AK, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MD, MI, MO, NC, NE, NH, NJ, NM, NV, NY, OH, OK, PA, TN, TX, UT, VA, WA, WI,and  WV, and the countries of ARGENTINA, CANADA, CHILE, CZECH REPUBLIC, FRANCE, GERMANY, GREECE, HONG KONG, HUNGARY, IRELAND, ITALY, JAPAN, NEW ZEALAND, PORTUGAL, RUSSIA, SAUDI ARABIA, SLOVAKIA, SPAIN, and UNITED KINGDOM.",
      "recall_number": "Z-1248-2015",
      "product_description": "GE Healthcare Proteus XR/a with wall stand model number 2260354.    Intended for use in generating radiographic images of human anatomy in all general purpose diagnostic procedures. This device is not intended for mammographic applications.",
      "product_quantity": "192 (131 US, 61 OUS).",
      "reason_for_recall": "Potential breakage of the steel cable which supports the bucky device in certain wall stands of Proteus XR/a X-ray imaging systems. A fall of a bucky while the system is in use could result in an injury to a patient or operator.",
      "recall_initiation_date": "20150130",
      "center_classification_date": "20150306",
      "termination_date": "20150915",
      "report_date": "20150318",
      "code_info": "Mfg Lot or Serial # System ID  00000014277HL8 503246PRO  00000014127HL5 202715PRO  00000013133HL4 206215RM1  00000013085HL6 206543HECED  00000014123HL4 208785RAD  00000014689HL4 208882GX1A  00000010591HL6 208893RAD2  00000014556HL5 209943SJRM2  00000013410HL6 214320RAD1  00000014413HL9 215918RAD1  00000014555HL7 215918RAD1  00000014684HL5 215918RAD2  00000014116HL8 216343R3  00000014276HL0 216343R4  00000013780HL2 217258SR3  00000024745HL2 217333LXR2  00000014020HL2 219284PRO1  00000014687HL8 225638R1  00000014119HL2 248652PROT3  00000014679HL5 262321RAD1  00000015410HL4 281392PRO  00000014424HL6 304257PROT  00000011358HL9 304354PROD  00000015166HL2 309655FNCR1  00000015168HL8 309655FNCR2  00000012515HL3 313369PROT  00000013910HL5 314768MRM8  00000014562HL3 314966JRM2A  00000011363HL9 318425LR1  00000013785HL1 319382PROTXR  00000014412HL1 330270PX  00000015409HL6 330438R3  00000014282HL8 330489XR3  00000014423HL8 330675PX  00000011060HL1 336768OSAB  00000010841HL5 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    }
  ]
}