Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a Recalled by Remote Diagnostic Technologies Ltd. Due to Due to incorrect labels applied to devices during...

Date: October 28, 2024
Company: Remote Diagnostic Technologies Ltd.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Remote Diagnostic Technologies Ltd. directly.

Affected Products

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

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Remote Diagnostic Technologies Ltd.

Remote Diagnostic Technologies Ltd. has 12 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report