Remote Diagnostic Technologies Ltd.: Philips Tempus LS-Manual Defibrillator
Recall reason: 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.. Recalled by Remote Diagnostic Technologies Ltd.. Distribution: US Nationwide distribution including in the states of VA, DC, MA, WY, AZ, FL, CA, NM, NJ, TN, OH, KS, IN, NY, IL, TX, NV, NE, PA, AL, IA, GA, MO, KY, WI, OR, CO, WV, WA, ET, UT, ID, OK, MN, ME, MT, MI, NC, ND, MD, DE, VT.. Classification (Class II — potential health risk). Affected lots/dates: 00-3020: UDI-DI-07613365002737
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