Class III

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

Remote Diagnostic Technologies Ltd. · October 28, 2024

Reason for Recall

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

Distribution

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

States Affected

NATIONWIDE

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0557-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.