Philips Recalls BrightView Imaging Systems
Philips has recalled its BrightView SPECT imaging systems for a potential component failure that would cause parts to fall on the patient.
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Philips Recalls Panorama 1.0T HFO MRI System for Explosion Risk
Philips is recalling the Panorama 1.0T HFO due to risk of explosion during a quench procedure caused by excessive pressure buildup.
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Philips Recall Sparks 48K Complaints to FDA in Three Months, Including 44 Deaths
The FDA updated a safety communication regarding the ongoing recall issues of Philips’ respiratory devices.
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Philips Files Lawsuit Against PSN Labs Over Foam Recall Damage
Philips has filed a lawsuit against PSN Labs, claiming incorrect analysis of foam material used in recalled ventilation devices.
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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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