Inquiry

list of knee replacement recalls

Exactech Fails to Adequately Inform Public of Faulty Knee

Jan 29, 2018 · What’s more, ever since 1994, when their Optetrak Total Knee Replacement System was first approved by the FDA, the company has continually recreated the product through a series of 510(k) premarket notifications, which, it should be known, don’t require any thorough testing. Instead, under these agreements, companies merely have to provide

Learn More

2018 Medical Device Recalls | FDA

The list below contains recalls that were issued in 2018. 2018 Recalls. Device Name Date; GE Healthcare Recalls CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing

Learn More

Video on What Happens During Knee Replacement Surgery

Dec 19, 2019 · A knee replacement may become necessary if one or both of your knees are damaged from arthritis or injury. Learn how a surgeon performs this

Learn More

Zimmer Recalls Knee Replacement Device

Zimmer Recalls Knee Replacement Device May 5, 2015 | Jonathan Rosenfeld Portions of the Zimmer Persona total knee replacement system is being recalled by its manufacturer. In February 2015, Zimmer, a leading orthopedic company, notified customers of its Class 2 FDA recall.

Learn More

Bone Cement Flaws May Lead to Knee Replacement Failure | Top

Jun 21, 2019 · Although knee replacement failure may be associated with implant defects, problems with surgical bone cement may also contribute to problems. During knee replacement surgery, bone cement is often used to help attach the implant to the natural bone. Bone cement comes in three viscosities: low, medium, and high.

Learn More

Medical Device Recalls

EMPOWR Partial Knee Peg Drill; Model: 800-06-008. 2 11/20/2020 Encore Medical, LP EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007. 2 11/20/2020 Encore Medical, LP Mako Integrated Cutting System (MICS) Handpiece, Catalog Number 209063, Software Version#: THA 3.0 a 2 11/19/2020

Learn More

Knee Replacement Lawsuit & Recall | My Vaccine Lawyer

Knee replacement implant lawsuit. Knee replacement is a fairly common procedure, and unfortunately, lawsuits from defective knee replacement devices are becoming just as common. The number of people with knee replacements has doubled over the last ten years. Joint replacement is now a $7 billion industry.

Learn More

Stryker Corporation – History, Products, Lawsuits and Recalls

Stryker is a global medical technology company. It makes hip replacement implants and surgical instruments, among other products. Stryker has had to recall some of its products because of concern for patient safety. The company has paid billions of dollars to end metal-on-metal hip implant lawsuits.

Learn More

Smith & Nephew Knee Replacement | Personal Injury Attorneys

Apr 10, 2015 · The FDA announced a Smith & Nephew recall of nearly 40,000 defective tibial baseplates in January 2010. An Alabama man filed a lawsuit against the manufacturer after receiving a knee replacement in 2008 which included a Journey tibial baseplate. The baseplate broke within 2 years of the replacement surgery.

Learn More

DePuy Knee Replacement Recalls and Litigation | Saunders

Learning of the alarming number of knee replacement recalls made by DePuy comes as no surprise to me. The company, a subsidiary of Johnson & Johnson, was deeply involved in the metal-on-metal hip replacement recall - the largest medical device failure in history. In recalling their ASR and Pinnacle metal-on-metal hip implant devices DePuy was

Learn More

Class 2 Device Recall DePuy P.F.C. Sigma Knee System

May 07, 2009 · Recall Status 1: Terminated 3 on October 25, 2010: Recall Number: Z-1686-2009: Recall Event ID: 52088: 510(K)Number: K943462 Product Classification: Prosthesis

Learn More

Knee Replacement Settlements Reached in Remaining Zimmer

Had knee replacement surgery in 2012 suffered for 6 years new knee just 2 months post op no pain at all. However having to have another replacement surgery is ridiculous. Sandra July 18, 2019 at

Learn More

10 Reasons Not To Trust Stryker For Your Knee Implant

You may or may not have heard about the FDA bringing the hammer down on Otismed, a subsidiary of Stryker the big knee replacement implant industry giant. In a nut shell, the CEO plead guilty to selling the The Otisknee, a cutting guide that helps surgeons align a "Custom knee" after the FDA denied the device 510K approval.

Learn More

Best Total Knee Replacement Blogs of 2020 - Healthline

Jun 12, 2020 · BoneSmart offers advocacy for people considering, undergoing, or recovering from knee replacement surgeries. Articles and FAQs on the blog cover all aspects of the

Learn More

Smith & Nephew Knee Replacement | Implant Failure & Lawsuits

Your first generation Smith & Nephew Journey Bi-cruciate Stabilized (BCS) Knee replacement system (Journey I BCS Knee System) may be defective. The manufacturer issued a voluntary recall in June of 2018, but phased this model out of production five years ago.

Learn More

Recalls on the Stryker knee - Printable Version

Recalls on the Stryker knee - Bummer Knees - 04-21-2010 I had a total knee replacement in 2008. My knee was in very bad shape before the surgery, as I was homebound much of the time due to the unstability & pain with this knee Today my knee is much improved, I can walk without the knee collasping.

Learn More

Zimmer NexGen Knee Recall Lawyers - Zimmer Recalled Knee

Following reports of at least 114 Zimmer NexGen knee replacement problems, the manufacturer issued a recall for Zimmer NexGen MIS Tibial Components, NextGen TM Tibial

Learn More

Zimmer recalls over 40,000 NexGen Total Knee Replacements

Your Dashboard for the Zimmer-Biomet Merger OVER 40,000 ZIMMER NEXGEN KNEE TIBIAL COMPONENTS RECALLED (Orthopedics This Week) Zimmer Holdings, Inc. is recalling 41,180 stemmed tibial components of the NexGen Complete Knee Solution system. According to an FDA Enforcement Report for the week of July 9, 2014, the company is initiating a voluntary recall of specific identified lots “due to the

Learn More

Class 2 Device Recall Vanguard Total Knee System

Jan 04, 2017 · The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.

Learn More

List of knee replacement recalls" Keyword Found Websites

Knee Replacement Implant Recall List - HealthClues Healthclues.net Why are some Knee replacement implants recalled? The most common reason for knee replacement implant recall is reported adverse events linked to a manufacturing defect of an implant, such as: Premature implant failure or loosening.

Learn More