GE Medical Systems, LLC Revolution XR/d systems with control room PC model 5117866-2 with Software collector 5194381. GE Healthcare, 3000 North Grandview, Waukesha, WI 53188. Intended for use in generating Tomographic images of human anatomy. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Revolution XR/d systems with control room PC model 5117866-2 with Software collector 5194381. GE Healthcare, 3000 North Grandview, Waukesha, WI 53188. Intended for use in generating Tomographic images of human anatomy.
Brand
GE Medical Systems, LLC
Lot Codes / Batch Numbers
and 0850070738.
Products Sold
SYSTEM 418525XRD 905575XRD 630856QXI 847437GEXRD3 847437XRDCH 605622RAD 850208XRD 217223XRD 269657XRD 415600XRD3 724873XRDL 615342ERXRD 615342RM1 205939SVXRD 716250RAD1 919575FCI2 919575LSCI 724458XRD 850934XRD 303932XRD 303932XRD 760241XRD 256265XR2 256265XR3 256IXR1 251435XRD1 208743LXRDX 318675ACCR1 318675ACCR2 708783R8 602506XRD 724773XRDL 843573WAXRD 713605XRD 562424XRD 954987PED1 713790MMXRD1 281274XRD2 865481FTXRD 630236XRD 949364ER 210646LXRD 781344XRD 567661XRD 630978XRDE185 630978XRDE186 805494XRD 847429ERT 440816XRD1 253952XRD1 314251JDRM4 636947XRDER 205408SVXRD 813654XRD 715393XRD 330841XRD7 330841XRD9 209669XRD 209669XRD 812238UH2 216844PEDR2 910822VAXRD2 205387WDC 503315WOXRD 803776VR1 XQ0068 XK0002 XK0003 XQ0076 XK0005 XK0006 XK0007 XK0001 082407040266 082407160202 0853070321 0850070730 0850070733 0850070734 0850070735 0850070736 0850070731, and 0850070738.
GE Medical Systems, LLC is recalling Revolution XR/d systems with control room PC model 5117866-2 with Software collector 5194381. GE Hea due to GE Healthcare has recently become aware of an error in the generator software on the Revolution XR/d configured with HP 8200 PC consoles that reports . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
GE Healthcare has recently become aware of an error in the generator software on the Revolution XR/d configured with HP 8200 PC consoles that reports a mAs reading that is higher than is actually exposed to patients.
Recommended Action
Per FDA guidance
Consignees were sent a GE Healthcare "Product Safety Notification" letter dated March 7, 2008. The letter was addressed to Hospital Administrators, Mangers of Radiology, and Radiologists. The letter listed the Safety Issue, Affected Product, Safety Instructions, and Contact Information.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, CA, CO, FL, ID, IL, IN, LA, MA, MI, MO, NY, NC, OH, OR, PA, SC, SD, TN, TX, WA, WI
Page updated: Jan 10, 2026