Les programmes de soutien par des pairs et la santé mentale chez les jeunes
Wed, 13 Oct 2021 10:11:27 -0400
Italiano
Wed, 13 Oct 2021 10:11:27 -0400
The FDA provides updated information from our ongoing evaluation of NTM infections in patients who have had cardiothoracic surgery using heater-cooler devices.
Tue, 12 Oct 2021 10:06:38 -0400
Tue, 12 Oct 2021 10:06:35 -0400
How to optimize dose accuracy when using ENFit LDT syringes – recommendations for patients and health care providers
Buena, NJ, Teligent Pharma, Inc. is voluntarily recalling the five lots of Lidocaine HCl Topical Solution 4%, 50ml in a screw cap glass bottle listed in the table below to the user level. The product is being recalled because the firms testing has found it to be super potent based on an Out of Speci
The FDA warns public and health care providers not to use needle-free devices for injection of dermal fillers.
The FDA is providing updated recommendations to help protect patient safety and reduce the risk of adverse events associated with surgical staplers.
DeRoyal Industries Recalls Procedure Packs Containing NORMOFLO Irrigation Warming Set Due to the Possibility of Harmful Levels of Aluminum Leaching
Imperative Care is recalling ZOOM 71 Reperfusion Catheter, used to remove blood clots in the brain, due to risk of breaking during use.
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