ClearanceBrief
Recall Z-2382-2016 ยท JAK System, X-Ray, Tomography, Computed

Philips Medical Systems (Cleveland) Inc

Brilliance iCT SP Model No. 728311; To produce cross-sectional images of the body.

DateApr 29, 2016
StatusTerminated
ReasonSoftware issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP products that could affect the performance of the equipment.
Root causeSoftware design
ActionThe customers will be sent a letter with information about, what the problems are and under what circumstances they may occur, the actions customers can take to minimize the effect of the problem and the actions planned by Philips to correct the problem. To correct these issues, a Philips field service representative will install a software update on the affected systems. Reference field change order (FCO) 72800652.
Quantity57 Units
DistributionProduct was shipped to the following states: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WV & WY. Product was also shipped to the following countries: Argentina, Australia
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K060937BRILLIANCE VOLUME
Philips Medical Systems (Cleveland), Inc., Jun 5, 2006