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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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Powerheart 9300A automated external defibrillator.
This fully automatic model does not require the ...
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2
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04/06/2010
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Cardiac Science Corporation
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Powerheart 9300E automated external defibrillator.
This semi-automatic model requires the user to...
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2
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04/06/2010
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Cardiac Science Corporation
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Powerheart 9300P automated external defibrillator.
This semi-automatic model requires the user to...
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2
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04/06/2010
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Cardiac Science Corporation
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Powerheart 9390A automated external defibrillator.
This fully automatic model does not require th...
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2
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04/06/2010
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Cardiac Science Corporation
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Powerheart 9390E automated external defibrillator.
This semi-automatic model requires the user to...
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2
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04/06/2010
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Cardiac Science Corporation
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Unilect ECG Electrodes
Unomedical, McAllen Texas.
Intended use:Cardiac monitoring
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2
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04/22/2010
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ConvaTec
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Responder 2000 Defibrillator/Monitor
Models: 2025653, 2026109, and 2026114.
Intended use: The Re...
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2
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05/26/2010
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Cardiac Science Corporation
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GE Healthcare, CARESCAPE" Monitor B850, Software version 1.0.1.13 and 1.0.2.1
The CARESCAPE " Mo...
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2
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06/11/2010
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Ge Healthcare, Llc
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Intesys Clinical Suite (ICS) G2 92810 Smart Disclosure. The Smart Disclosure product collects patie...
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2
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08/25/2010
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Spacelabs Healthcare, Incorporated
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3M Red Dot Monitoring Electrode, Catalog #2560 & Novaplus Universal Monitoring Electrode #V2560, use...
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2
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09/07/2010
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3M Company / Medical Division
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