Remote Diagnostic Technologies Ltd. 2023-04-12 Health serious FDA
Health · FDA · Recall #FDA-Z-1321-2023
Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by… Recall
Issued April 12, 2023 · Remote Diagnostic Technologies Ltd.
In April 2023, Remote Diagnostic Technologies Ltd. recalled the Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
During internal testing, Regulatory Compliance issues were identified regarding the Monitor and Power Supplies for fluid ingress and basic safety issues.
What you should do
- 1 Stop using Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by… 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
- April 12, 2023
- Units affected
- Not reported
- Sold at
- 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
- Recall number
- FDA-Z-1321-2023
- 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.