Remote Diagnostic Technologies Ltd. 2023-06-21 Health serious FDA
Health · FDA · Recall #FDA-Z-1825-2023
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 Recall
Issued June 21, 2023 · Remote Diagnostic Technologies Ltd.
In June 2023, Remote Diagnostic Technologies Ltd. recalled the Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Defibrillator/pacemaker module (DPM) may encounter a problem causing communication from the Mainboard to the DPM to fail, leading to no or ineffective pacing with displayed error message "HW failure DPM".
What you should do
- 1 Stop using Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 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
- June 21, 2023
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of UT, CO, CA, NE, IL, TX, WV, KS, GA.
- Recall number
- FDA-Z-1825-2023
- 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 903rd Health recall we've logged in 2023.