Philips Medical Systems Intellivue Central Station Software for the: Intellivue Information Center; Philips Information Center, Central Station Models: M3145, M3150, M3154, M3155, M3169 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Intellivue Central Station Software for the: Intellivue Information Center; Philips Information Center, Central Station Models: M3145, M3150, M3154, M3155, M3169
Brand
Philips Medical Systems
Lot Codes / Batch Numbers
"Service" 2-Under the "Other Services " menu item, click "Software Versions" 3-"Application" lists the application software version.
Products Sold
Software versions: J.00.23 and J.00.24 (You can determine the application software release as follows: 1-Enter Service Mode through "All Controls" , "Service" 2-Under the "Other Services " menu item, click "Software Versions" 3-"Application" lists the application software version.
Philips Medical Systems is recalling Intellivue Central Station Software for the: Intellivue Information Center; Philips Information Cent due to Incorrect Patient Assignment: the information center will in most cases be associated with the "incorrect" patient. This occurs on both standalone an. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect Patient Assignment: the information center will in most cases be associated with the "incorrect" patient. This occurs on both standalone and networked systems running fixed mode monitoring. (This does not occur on systems that run flex mode monitoring)
Recommended Action
Per FDA guidance
Philips Medical Systems issued a letter notification dated July 2007 " Urgent Device Correction". Customers with networked information centers will be corrected through a database server. Stand-Alone units will have a software correction. Software version J.00.25 will correct the problem. Users are advised not to use th 12 Lead Analysis and Export Option in fixed or flex mode monitoring unitl the software correction is made.
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
MI, NJ, NY, OK, UT
Page updated: Jan 10, 2026