Philips Medical Systems (Cleveland) Inc Brilliance CT System 6/10/16/16P/40 configuration. No packaging, sold as single unit. Computed tomography scanner intended to provide cross sectional images of the human body and visualization of the internal organs. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Brilliance CT System 6/10/16/16P/40 configuration. No packaging, sold as single unit. Computed tomography scanner intended to provide cross sectional images of the human body and visualization of the internal organs.
Brand
Philips Medical Systems (Cleveland) Inc
Lot Codes / Batch Numbers
728256, 728251, 728246, 728240, and 728235.
Products Sold
728256, 728251, 728246, 728240, and 728235.
Philips Medical Systems (Cleveland) Inc is recalling Brilliance CT System 6/10/16/16P/40 configuration. No packaging, sold as single unit. Computed t due to The system has a gap that can appear between the upper and lower tilt stand covers. The fingers may be squeezed if a person was to place them in this . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The system has a gap that can appear between the upper and lower tilt stand covers. The fingers may be squeezed if a person was to place them in this region while the gantry was tilting from an angle to zero tilt angle.
Recommended Action
Per FDA guidance
Customers will be contacted by a field service technician with the field correction order. The firm will install the new labeling to the device.
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
AZ, CO, GA, IL, IN, IA, KS, KY, MD, MI, MN, MS, NY, NC, OH, OK, TX, VT, WI
Page updated: Jan 10, 2026