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 man

Recalled December 4, 2024 · FDA recall Z-0557-2025 · Remote Diagnostic Technologies

Hazard

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

Sold at

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

Description

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

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

Manufacturer(s)

Remote Diagnostic Technologies Ltd.

Made in

United Kingdom

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →