Remote Diagnostic Technologies Ltd. recalls Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or…
Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.
Read the official notice →- Date
- 2024-12-04
- Country
- United States
- Brand
- Remote Diagnostic Technologies
- Product
- Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode
- Classification
- Class III
- Units
- U.S. Nationwide distribution in the states of AL, CA, FL, MO, NY, OH, TX and VA.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Remote Diagnostic Technologies recalls
- 2025-08-06
USRemote Diagnostic Technologies Ltd. recalls Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an…
Kit USB flash drive contains outdated software, which could result in reverting patient monitor to outdated software and reintroducing the video laryngoscope issue (related to an August 2023 recall), which could lead…
FDA · DeviceRemote Diagnostic Technologies Ltd.Worldwide - US Nationwide distribution in the states of SC, KY, NV, IA, MI and…Official notice →- 2025-05-14
- US
Remote Diagnostic Technologies Ltd. recalls Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007
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…
FDA · DeviceRemote Diagnostic Technologies Ltd.Worldwide - US Nationwide distribution including in the states of AZ, VA, FL,…Official notice → - 2025-04-30
- US
Remote Diagnostic Technologies Ltd. recalls Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007…
software issue that causes an error screen on a portable vital signs monitor when attaching video Laryngoscope.
FDA · DeviceRemote Diagnostic Technologies Ltd.Worldwide - US Nationwide distribution including in the states of AL, AZ, CA,…Official notice → - 2024-06-12
- US
Remote Diagnostic Technologies Ltd. recalls Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual
Simultaneous ECG measurements with multiple devices, including a manual defibrillator, on the same patient may cause electrical noise or interference, which may lead to distortions of the ECG signal; distortions may…
FDA · DeviceRemote Diagnostic Technologies Ltd.US Nationwide distribution including in the states of VA, DC, MA, WY, AZ, FL,…Official notice → - 2023-09-27
- US
Remote Diagnostic Technologies Ltd. recalls Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used With…
Full screen error message may occur on patient monitors with affected hardware version, either during or after laryngoscopes are unplugged from monitors, informing users a 60-100 second shutdown/restart are required.…
FDA · DeviceRemote Diagnostic Technologies Ltd.US:AZ, AL, CA, CO, DC, DE, FL , GA, HI, IA, ID, IL, IN , KS, KY, MA , MD , ME,…Official notice → - 2023-06-21
- US
Remote Diagnostic Technologies Ltd. recalls Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
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".
FDA · DeviceRemote Diagnostic Technologies Ltd.US Nationwide distribution in the states of UT, CO, CA, NE, IL, TX, WV, KS, GA.Official notice →
Other drugs & medical recalls in the United States
- 2024-12-04
- US
Securitas Healthcare LLC recalls Arial Server Software Versions 11.1.4 through 11.1.6, SKU 54305, in conjunction with the Arial Mobile Application or Arial Care Giver…
Certain software versions will not notify end users of calls initiated by call points with the Arial Emergency and Nurse Call System.
FDA · DeviceSecuritas Healthcare LLCWorldwide distribution - US Nationwide and the countries of Canada, Switzerland.Official notice → - US
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
- US
MEDLINE INDUSTRIES, LP - Northfield recalls ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case; Medline Convenience Kits containing Single Use…
Identified lots of Olympus product may be missing sterile and manufacturing lot numbers and expiration dates on the sterile packaging. The information can be found on the outer box or zipper bag label. Medline is…
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of NY.Official notice → - US
Shimadzu Corp. Analytical & Measuring Instruments Div. recalls Autosampler, Models: SIL-40C XR CL, SIL-40C X3 CL
There have been cases of failure of the main board due to condensation water occurring in the gap between thermal insulation material on the underside of the main base dropping onto the main board The symptoms and…
FDA · DeviceShimadzu Corp. Analytical & Measuring Instruments Div.Worldwide - US Nationwide distribution in the states of DE, PA and the country…Official notice → - US
Shimadzu Corp. Analytical & Measuring Instruments Div. recalls Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL
There have been cases of failure of the main board due to condensation water drained from the Peltier dehumidifier, leaked out from the tray, resulting in a short circuit. In the serious case, the main board and…
FDA · DeviceShimadzu Corp. Analytical & Measuring Instruments Div.Worldwide - US Nationwide distribution in the states of MS, AR, TX, CA, MA,…Official notice → - US
Abbott Medical recalls Merlin@home Transmitter REF EX1100 The Merlin@home" (M@h) transmitter is intended to transfer stored data from the patient s implanted…
Due to heart transmitter not being able to upgrade to the current software version in the field after experiencing a power interruption during a prior over-the-wire software download.
FDA · DeviceAbbott MedicalWorldwide - U.S. Nationwide distribution in the states of ALABAMA, ALASKA,…Official notice →