Remote Diagnostic Technologies Ltd.: Medical Device Recall in 2024 - (Recall #: Z-0557-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode

Product Classification:

Class III

Date Initiated: October 28, 2024

Date Posted: December 4, 2024

Recall Number: Z-0557-2025

Event ID: 95642

Reason for Recall:

Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.

Status: Ongoing

Product Quantity:

Code Information:

Model Number: 00-3020 UDI-DI code: 07613365002737 Serial Numbers: 7022.000367 7022.000387 7022.000392 7022.000462 7022.000463 7022.000464 7022.000559 7022.000591 7022.000595 7022.000711 7022.000781 7022.000786 7022.00108 7022.001175 7022.001201 7022.00129 7022.001556 7022.001582

Distribution Pattern:

U.S. Nationwide distribution in the states of AL, CA, FL, MO, NY, OH, TX and VA.

Voluntary or Mandated:

Voluntary: Firm initiated