Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic Technologies Ltd. Due to Defibrillator/pacemaker module (DPM) may encounter a problem causing...
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
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
Quantity: 1147
Why Was This Recalled?
Defibrillator/pacemaker module (DPM) may encounter a problem causing communication from the Mainboard to the DPM to fail, leading to no or ineffective pacing with displayed error message "HW failure DPM".
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