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 Simultaneous ECG measurements with multiple devices, including a...
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 when using Tempus LS-Manual User/Operator Manual
Quantity: 1745
Why Was This Recalled?
Simultaneous ECG measurements with multiple devices, including a manual defibrillator, on the same patient may cause electrical noise or interference, which may lead to distortions of the ECG signal; distortions may lead to no or ineffective pacing, or no or inappropriate defibrillation pulse.
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