Remote Diagnostic Technologies Ltd.: Medical Device Recall in 2023 - (Recall #: Z-1825-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020

Product Classification:

Class II

Date Initiated: May 8, 2023

Date Posted: June 21, 2023

Recall Number: Z-1825-2023

Event ID: 92251

Reason for Recall:

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".

Status: Ongoing

Product Quantity: 1147

Code Information:

UDI-DI: 07613365002737. Serial numbers prior to 7022.001634

Distribution Pattern:

US Nationwide distribution in the states of UT, CO, CA, NE, IL, TX, WV, KS, GA.

Voluntary or Mandated:

Voluntary: Firm initiated