JIANGSU JUMAO X-CARE Medical Equipment Co. issued a recall for the JMC5A Ni/Tru-Aire-5 Oxygen Concentrator after incidents of spontaneous fires. These fires could cause burns or worse. Patients are ...
The FDA labeled a recall of integrated arterial catheters made by Medline Class I, the most serious kind of recall.
Following a recall of grounding pads produced by Megadyne, a machinery industry company, the FDA is notifying veterinarians ...
The U.S. Food and Drug Administration has issued an urgent recall for the JMCC5A Ni/TruAire-5 Oxygen Concentrator due to the device spontaneously catching fire.
The company will keep the systems on the market but is asking providers to check devices for visible cracks and return ...
The FDA has recalled Mercury Medical’s Neo-Tee T-Piece Resuscitator, a gas powered resuscitator intended primarily for ...
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FDA issues cybersecurity risk alert over Contec patient monitorThe FDA says the cybersecurity vulnerabilities identified may put patients at risk when the device is connected to the internet.
Susan Krause of Rosemount alleges New Jersey-based Integra LifeSciences pressured her to lie to regulators. Integra says ...
Olympus Corporation has announced a voluntary Advisory Notice for the Forceps/Irrigation Plug (Isolated Type) model MAJ-891 related to the risk of device contamination that may result from improper ...
These strategies can create a healthcare ecosystem that prioritizes patient safety, empowers consumers with information and ...
The website changes raise concerns about “the interference of politics with the study and the practice” of science and ...
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