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Remote Diagnostic Technologies Ltd. Recall: Philips Tempus Pro Patient Monitor, REF: 00-10

Remote Diagnostic Technologies Ltd. Recall: Philips Tempus Pro Patient Monitor, REF: 00-10 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Remote Diagnostic Technologies Ltd.; Product: Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007

Recalling firmRemote Diagnostic Technologies Ltd.
ProductPhilips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007
Reason for recallPatient Monitor software update to address issues:1)May freeze at startup with MPM Application error and Attention Restart Required messages,2)Monitor may freeze and reboot at start of 12-lead ECG or after, 3)May reboot after intermittent connection with Smart Mount, 4) 12-lead ECG measurements with Louvain algorithm and software before vx.36 could produce inaccurate rhythm/morphology statements.
ClassificationClass II (moderate — may cause temporary or reversible health consequences)
StatusOngoing
DistributionWorldwide - US Nationwide distribution including in the states of AZ, VA, FL, CA, TX, NM, IA, NJ, TN, OH, KS, IN, NC, IL, WY, WI, NV, NY, NE, PA, AL, , MA, GA, MO, CO, OK, KY, OR, MS, MI, HI, WA, UT, WV, ID, ND, NH, MN, MT, ME, MD, DE, DC and the countries of AU, GB, IT, SA, DE, AE, BO, FR, ES, BE,
Recall initiated20250415
Recall numberZ-1729-2025
Categorydevice
StateN/A
CountryUnited Kingdom

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