Le point sur l’examen des médicaments — numéro 44
Italiano
Megadyne issued a Class 1 Medical Device Correction to hospitals to limit the use of MEGA SOFT Universal and Universal Plus Reusable Patient Return Electrodes to patients aged 12 years or older after receiving reports of adult and pediatric patient burns following surgical procedures in which MEGA S
Problems may occur if electrical operating room table best practices are not followed. Read the FDA’s recommendations to avoid complications.
Wipro Ge Healthcare Private Ltd. is recalling its Care Plus and Lullaby Incubators because the bedside panel or porthole may not latch properly.
Learn more about recommendations for patients who are considering a Hintermann Series H3 TAR system or who have one; recommendations for health care providers.
Les injections d’eplontersen sont indiquées dans le traitement de la polyneuropathie associée à l’amylose héréditaire à transthyrétine (ATTRh) chez l’adulte.
In direct response to the Nurse Assist, LLC voluntary recall of pre-filled syringes and other sterile water products, Avanos Medical, Inc. (NYSE: AVNS) voluntarily recalled specific lots of MIC* Gastric – Jejunal Feeding Tube Kits on Jan. 16, 2024. These kits include Nurse Assist supplied syringes,
FDA is informing the public of adverse events reported with the use of BioZorb Marker including pain, migration, erosion, and others.
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