Remote Diagnostic Technologies Ltd. 2025-05-14 Health serious FDA
Health · FDA · Recall #FDA-Z-1729-2025
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R,… Recall
Issued May 14, 2025 · Remote Diagnostic Technologies Ltd.
In May 2025, Remote Diagnostic Technologies Ltd. recalled the Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Patient 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.
What you should do
- 1 Stop using Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Remote Diagnostic Technologies Ltd. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Remote Diagnostic Technologies Ltd.
- Category
- Health
- Recall date
- May 14, 2025
- Units affected
- Not reported
- Sold at
- Worldwide - 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
- Recall number
- FDA-Z-1729-2025
- Made in
- United Kingdom
- Issuing agency
- FDA
In context
- Remote Diagnostic Technologies Ltd. has 3 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.