Search results
Results from the WOW.Com Content Network
Options for mesh include either synthetic or biologic. Synthetic mesh provides the option of using "heavyweight" as well as "lightweight" variations according to the diameter and number of mesh fibers. [34] Lightweight mesh has been shown to have fewer complications related to the mesh itself than its heavyweight counterparts. [35]
Prolene is a brand of synthetic polypropylene used in monofilament nonabsorbable sutures and meshes. The suture is indicated for skin closure and general soft tissue approximation and ligation. Its advantages include minimal tissue reactivity and durability.
These databases are some of the largest of their kind, [1] and even the largest ever. [2] Accessibility of government databases may be controlled by various means, such as requirement of a warrant, subpoena, or simple request from another branch of government. Commercial databases are generally established for profit.
A cucumber recall under investigation by the U.S. Centers for Disease Control and Prevention (CDC) has led to over 400 illnesses due to contamination with the bacteria salmonella.
Costco Recalls. Costco continues pulling products off its shelves as a wave of listeria contamination sweeps the country. Within the past week, the wholesale giant sent separate notices to its ...
The Food and Drug Administration (FDA) said in its recall alert that listeria monocytogenes is “an organism that can cause serious and sometimes fatal infections in young children, frail or ...
Surgical mesh is implanted to strengthen tissue repair and minimize the rate of recurrence. The surgery can be performed laparoscopic (internally) or open with a variety of materials available for prosthesis. [4] Polypropylene (PP) is the most frequently used type of mesh, although it may be uncomfortable for the patient after implantation.
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.