Tempus Pro Patient Monitor Software Error: Error Screen When Attaching Video Laryngoscope
Remote Diagnostic Technologies recalls Tempus Pro Patient Monitors with specific model numbers due to a software error causing error screens when attaching video laryngoscopes. Affected units may display errors during use.
Lower-risk recall
software issue that causes an error screen on a portable vital signs monitor when attaching video Laryngoscope.
Contact the company
What happened, in plain English
Remote Diagnostic Technologies is recalling certain Tempus Pro Patient Monitors because a software issue causes error screens when attaching video laryngoscopes. This could lead to incorrect vital sign readings during medical procedures. Read more at govinfonow.com/recall/52450-tempus-pro-patient-monitor-software-error-error-screen-when-attaching.
Source Summary by GovInfoNow · govinfonow.com/recall/52450-tempus-pro-patient-monitor-software-error-error-screen-when-attaching · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1666-2025
Cite this page
“Tempus Pro Patient Monitor Software Error: Error Screen When Attaching Video Laryngoscope.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52450-tempus-pro-patient-monitor-software-error-error-screen-when-attaching. Based on FDA recall #Z-1666-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1666-2025%22&limit=1).
Why it’s dangerous
The software issue causes the monitor to display an error screen when a video laryngoscope is attached. This could result in incorrect vital sign readings during medical procedures, potentially affecting patient care.
Who’s affected
Healthcare providers using the Tempus Pro Patient Monitors with specific model numbers and serial codes are most at risk. Patients receiving care from these devices may be affected if the error screen occurs during procedures.
How to tell if you have this one
Check for model numbers 00-1004-R, 00-1007-R, 00-1007, 00-1024-R, 00-1026-R, or 00-1004 on the device. The serial numbers listed in the recall notice are also specific to affected units.
- Brand
Remote Diagnostic Technologies- Category
Medical device
What to do — step by step
Check Device Model
Identify the model number on your Tempus Pro Patient Monitor to see if it matches the recalled units.
Verify Serial Number
Check the serial numbers listed in the recall notice to confirm if your device is affected.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 42 states.
FDA distribution: “Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA, WI, WV, WY and…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Arizona, California, Colorado, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA published this recall 14 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using the device?
No, the recall does not require stopping use immediately. The device can continue to be used but may display an error screen when attaching video laryngoscopes.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1666-2025 (April 16, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1666-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.