Tempus Pro Patient Monitor Recall: Regulatory Compliance Issues with Power Supplies
Remote Diagnostic Technologies recalls Tempus Pro Patient Monitors with specific model numbers and UDI-DI codes due to regulatory compliance issues involving fluid ingress and basic safety risks in power supplies.
Lower-risk recall
During internal testing, Regulatory Compliance issues were identified regarding the Monitor and Power Supplies for fluid ingress and basic safety issues.
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What happened, in plain English
Remote Diagnostic Technologies is recalling Tempus Pro Patient Monitors with certain model numbers and UDI-DI codes because internal testing found regulatory compliance issues with the power supplies. This could lead to fluid ingress and basic safety risks, which may affect clinical use. Read more at govinfonow.com/recall/58851-tempus-pro-patient-monitor-recall-regulatory-compliance-issues-with-power.
Source Summary by GovInfoNow · govinfonow.com/recall/58851-tempus-pro-patient-monitor-recall-regulatory-compliance-issues-with-power · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1321-2023
Cite this page
“Tempus Pro Patient Monitor Recall: Regulatory Compliance Issues with Power Supplies.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58851-tempus-pro-patient-monitor-recall-regulatory-compliance-issues-with-power. Based on FDA recall #Z-1321-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1321-2023%22&limit=1).
Why it’s dangerous
The power supplies in the recalled units have regulatory compliance issues that could allow fluid ingress and basic safety risks. These issues may affect the device's performance and safety during clinical use, but the risk is not severe enough to cause serious injury in normal use.
Who’s affected
Clinicians and medically qualified personnel who use the Tempus Pro Patient Monitors for vital signs monitoring in clinical or pre-hospital care settings are most at risk. All units with the listed model numbers and UDI-DI codes are affected.
How to tell if you have this one
Check the model numbers: 00-1004, 00-1004-R, 00-1007, 00-1007-R, 00-1024-R, 00-1026-R. Also look for UDI-DI codes: 05060472440020, 05060472442901, 05060472440013, 05060472442901, 05060472441027, 05060472442925, 05060472441058, 05060472442932. All products manufactured are affected.
- Brand
Remote Diagnostic Technologies- Category
Medical device
What to do — step by step
Check Model Numbers
Identify if your Tempus Pro Patient Monitor has model numbers 00-1004, 00-1004-R, 00-1007, 00-1007-R, 00-1024-R, or 00-1026-R.
Check UDI-DI Codes
Look for UDI-DI codes: 05060472440020, 05060472442901, 05060472440013, 05060472442901, 05060472441027, 05060472442925, 05060472441058, or 05060472442932.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 41 states.
FDA distribution: “Worldwide Distribution: U.S.(nationwide): AL, AZ, CA, CO, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA, WI, WV, WY and O.U.S.(foreign): United…” 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, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, 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 48 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.
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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-1321-2023 (February 23, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1321-2023 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 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.