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Some Covidien ventilators are being recalled following reports they may shut off unexpectedly, which has already resulted in at least one patient death.
Philips Respironics is recalling more than 16,00 V60 and V60 Plus ventilators which may fail to supply enough oxygen to patients with high oxygen requirements in certain situations, which has already led to 25 patient injuries.
The FDA warns some 200,000 devices included in a recent Philips CPAP recall, including BiPAP machines and mechanical ventilators, may place patients at a greater risk, due to their role in keeping those patients breathing.
A GE Healthcare ventilation system recall announced by the FDA warns that failure of the system due to loose internal connections could result in severe injury or death for patients.
Problems with a Medtronic ventilator may cause the devices to reset while in use, preventing patients from receiving proper respiratory support.
A recall for VentStar Oxylog 3000 disposable pediatric patient circuits has been deemed by the FDA to be a Class I medical device recall because a leak could cause serious injury or death to children.
A recall of 251 eVent Inspiration ventilators has been issued due to reports that the devices shut down unexpectedly, which could endanger patients who need the device to breathe.
Puritan Bennett neonatal and adult ventilators are being recalled due to problems with delivering the correct amount of oxygen to patients.
The FDA warns that a asoftware problem linked to some Covidien ventilators could cause serious injury or death to patients.
Defective keypads have led to a recall of a number of GE Healthcare ventilators and anesthesia delivery systems because of problems that could put patients at risk.
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