Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic Technologies Ltd. Due to Full screen error message may occur on patient...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Remote Diagnostic Technologies Ltd. directly.
Affected Products
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used With Tempus Pro Video Laryngoscope, REF 01-2044
Quantity: 3,524
Why Was This Recalled?
Full screen error message may occur on patient monitors with affected hardware version, either during or after laryngoscopes are unplugged from monitors, informing users a 60-100 second shutdown/restart are required. Error prevents: viewing graphical patient vital signs, sounding of pulse audio tone, visualization of patient airway used during intubation; may lead to treatment delay or hypoxia.
Where Was This Sold?
This product was distributed to 42 states: AL, AZ, CA, CO, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NJ, NM, NY, NC, ND, OH, OK, OR, PA, TN, TX, UT, VA, WA, WV, WI, WY, DC
About Remote Diagnostic Technologies Ltd.
Remote Diagnostic Technologies Ltd. has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report