FDANovember 17, 2020device

Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.3.4 - Product Usage: The device is intended to be used in the following environmental: - Primarily in pre-hospital care and transport applications (including ambulances, fixed and rotary wing aircraft).

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

A software error was detected within software version 1.3.4 for the Tempus LS device. When exiting pacer back into manual mode the pacer pulse wave may put the ECG calibration out of calibration. This software error may result in a delay in therapy, as the clinician is not provided an ECG waveform on which a shockable rhythm decision can be made. The device is still able to deliver a manual defibrillation shock.

What to do

FDA enforcement status: Terminated

Brands named

remote diagnostic technologiesremoteremote diagnostic

UPCs

07613365002737

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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