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...
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.
About Remote Diagnostic Technologies Ltd.
Remote Diagnostic Technologies Ltd. has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report