Baxter Recalls Life2000 Ventilator for Battery Charging Issue
Baxter is recalling the Life2000 Ventilator System due to potential battery charging dongle failure, which can prevent or hinder charging.
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Search Results for: recall
FDA Classifies Philips, Baxter, and Zoll Ventilator Recalls as Class I
Three major manufacturers—Philips Respironics, Baxter Healthcare, and Zoll Medical—have issued Class I recalls for their ventilators due to critical issues posing a risk of serious injury or death.
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Medline Recalls Sub-G Endotracheal Tube for Choking Risk
Medline recalled the Sub-G Endotracheal Tube with Subglottic Suction due to risks of detachment, tearing, and potential airway obstruction.
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Abbott Recalls HeartMate 3 LVAS for Leakage Issue
Abbott is recalling the HeartMate 3 LVAS due to issues with blood leakage and air entrapment during implantation.
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TruAsset Integrates with Equiptrack for FDA Recalls
TruAsset has integrated with Equiptrack to enhance the efficiency of processing FDA recalls and streamline patient safety processes.
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