Certain Philips Respironics BiPAP Machines Recalled Due to a Plastic Issue, FDA Says
Philips recalled certain bi-level positive airway pressure machines that may contain a plastic contaminated with a non-compatible material.
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Search Results for: ventilator
Invictus Seeks to Commercialize NICU Active Noise Control Device
Invictus Medical has submitted a De Novo application to the FDA for its Neoasis incubator-based active noise control device.
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Getinge’s Recall of 11,000 Ventilators Labeled Class I Event by FDA
Getinge is recalling several different types of ventilators in its device portfolio that are being labeled as a Class I event by the FDA.
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Linamar MedTech Achieves ISO 13485 Certification for Medical Device Manufacturing
Linamar Corp., a diversified manufacturing company, announced its iHub production site has received ISO 13485 certification for medical device production.
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Medtronic Recalls Defibrillator Devices for Short Circuit Alert Risks
Medtronic is recalling Cobalt/Crome implantable cardioverter defibrillators and cardiac resynchronization therapy defibrillators.
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