Device recalls

IntelePACS (Image Fusion Module) - InteleViewer

INTELERAD MEDICAL SYSTEMS INCORPORATED · A software application that receives digital images and data from various sources has a bug in specific software versions that will calculate the Standard Upta…

Open, ClassifiedSoftware designZ-1208-2025
Open FDA's page for this record
Cfres ID
212457
Product res number
Z-1208-2025
Event date initiated
2025-02-05
Event date posted
2025-02-21
Recall status
Open, Classified
Res event number
96270
Product code
LLZ
Product description
IntelePACS (Image Fusion Module) - InteleViewer
Code info
UDI-DI: B228INTELEPACS0, Device Versions: 5-6-1-P23 and later
Firm FEI number
3003768392
Recalling firm
INTELERAD MEDICAL SYSTEMS INCORPORATED
Address 1
800, Boul. de Maisonneuve Est 800 Boul. de Maisonneuve Est
Address 2
12th floor
City
Montreal
Country
Canada
Root cause description
Software design
Product quantity
88
Reason for recall

A software application that receives digital images and data from various sources has a bug in specific software versions that will calculate the Standard Uptake Value (SUV) incorrectly for PET/CT studies acquired on the days of Daylight Savings Time (DST); only on dates in which DST transition occurs; all other dates are unaffected. An incorrect SUV may lead to an incorrect diagnosis.

Action

On 2/5/2025, correction notices were emailed to customers who were asked to do the following: The following work around can be completed for any impacted SUV calculation. The correct SUV values may be obtained in the SUV calculator, as follows: 1. Adjust the administration time and series time in IntelePACS consistent with the actual time of injection and the time of series acquisition. 2. Verify that the calculated elapsed time is correct. 3. Recalculate the SUV in the calculator, this is the correct SUV value. - Customers are asked to review scans and notify the recalling firm if scans were performed on Daylight Savings Time dates since 2022. - A software upgrade to eliminate this bug is expected to be released by the end of March 2025. Once available, you will be notified via email. You will then be able to schedule your product upgrade. - Complete and return the acknowledgement form via email to regulatory-affairs@intelerad.com For more information or to ask any questions about this notification, please contact the firm's regulatory affairs department at regulatory-affairs@intelerad.com

Distribution pattern

Worldwide - US Nationwide distribution in the states of AZ, NC, MI, FL, NH, WY, CA, SC, AL, AR, IN, MD, CO, TN, IL, NJ, OH, MN, WV, KE, NE, VA, WA, GE, WI and the countries of New Zealand, Canada, Australia

K numbers
K192176
Harmonized identifiers (openFDA)
Device name
System, Image Processing, Radiological
Medical specialty description
Radiology
Regulation number
892.2050
Device class
2
K number
K061696, K915305, K110573, K243697, K220727, K992925, K172477, K253111, K212981, K953616, K131246, K182624, K962153, K042634, K973983, K962589, K063006, K041990, K043146, K140139, K000770, K071331, K897000, K925963, K171314, K963697, K131822, K141570, K880169, K182904, K152602, K983821, K182230, K033849, K002942, K042507, K843708, K221984, K130395, K061029 +2,255 more
Registration number
3001052305, 3005406110, 3017545364, 3005172103, 9617978, 3004706313, 3008487708, 1226544, 3009341091, 3044776706, 3010656400, 3038189169, 3007362683, 3007993775, 1061158, 3014232555, 3003757027, 3014991167, 9617592, 3013634985, 3023217364, 1054415, 3013535906, 3026047529, 3019878658, 3005225421, 3030655434, 3009156722, 3010445368, 8020825, 3011676026, 3008364043, 3045521711, 3014635169, 2954921, 9615439, 3011015597, 3003989064, 3035371452, 3019544554 +603 more
FEI number
3001052305, 3005406110, 3017545364, 3005172103, 3004706313, 3008487708, 3009341091, 3044776706, 3002808188, 3010656400, 3038189169, 3007362683, 3007993775, 3014232555, 3003757027, 3014991167, 3013634985, 3023217364, 3013535906, 3026047529, 3019878658, 3005225421, 3030655434, 3009156722, 3010445368, 3011676026, 3008364043, 3045521711, 3014635169, 3011015597, 3003989064, 3035371452, 3019544554, 3008548323, 3014269683, 3002821504, 2126677, 3002619595, 3010684280, 3003861317 +603 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.