Ad
related to: hernia mesh recall fda
Search results
Results from the WOW.Com Content Network
On June 13, 2016, Health Canada issued a recall of Ethicon's Physiomesh Flexible Composite Mesh Product used for ventral hernia repair. [13] The product had been on the Canadian market since September 2010 and patients claimed a range of complications following surgery. [14]
As a drug delivery system, a hernia mesh can be used to deliver antibiotics, [23] antiseptics, [24] antimicrobials, [21] antimicrobial peptides [25] or nanoparticles. [26] Different techniques can be used to implement the integration of such substances, including dipping/soaking, physical coating, chemical surface functionalization and ...
SafeStitch Medical has developed and obtained FDA approval to market the AMID Hernia Fixation Device (HFD) for both inguinal and ventral hernia repairs. The AMID HFD allows for faster mesh ...
The tools were recalled by Megadyne Medical Products, which was acquired in 2017 by Ethicon Endo-Surgery, a US FDA classifies recall of J&J's electrosurgical tools as most serious Skip to main content
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]
The U.S. Food and Drug Administration has issued a Class I recall, the agency's most serious, for a Medtronic device used to temporarily drain spinal fluid from patients after surgery for a ...
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.
An investigation showed that Boston's device, Obsidio Embolic, when used with a specific technique posed a higher risk of bowel ischemia during procedures to stop gastrointestinal (GI) bleeding ...
Ad
related to: hernia mesh recall fda