trabecular metal recalled

Trabecular Metal Recalled

Class 2 Device Recall Persona Trabecular Metal Tibial ...

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 …

Trabecular Metal™ Technology | Zimmer Biomet

Trabecular Metal Material is made of elemental tantalum (atomic number 73), one of the most chemically stable and biologically inert metals used in orthopedic implants. 5 This makes it highly biocompatible and corrosion-resistant. Tantalum is the ideal material for this structure, because it has high fatigue strength and a compressive modulus that allows it to bend before breaking. 3

Zimmer Knee Replacement Recall and Joint Replacement Lawsuits

Mar 24, 2017 · Zimmer Recalls Persona Trabecular Metal Tibial Plate Knee Implant. Zimmer has launched several joint replacement recalls that may lead to product liability lawsuits. One recall affects a Zimmer knee implant; the Persona Trabecular Metal Tibial Plate was recalled due …

Class 2 Device Recall Zimmer Trabecular Metal

This single manufacturing lot has the potential for the bond strength between the Trabecular Metal material and substrate to be below the minimum required specification. Testing found bond strength approximately 80% of the minimum required by specification …

FDA Recalls Zimmer Trabecular Metal Modular Acetabular ...

(OPENPRESS) September 30, 2011 -- On September 27, 2011, US stone and Drug Administration (FDA) recalled the Trabecular Metal Modular Acetabular System manufactured by Zimmer Inc. The Trabecular Metal Modular Acetabular System is a modular acetabular cup system consisting of a shell with a preassembled locking ring, a liner, and optional screws.

FDA Issues Notice of Class 2 Recall for Zimmer Persona ...

Mar 27, 2015 · The FDA on March 12 issued a notice for a Class II Recall for all lots and sizes of the Zimmer Persona Trabecular Metal Tibial Plate knee implant. According to the agency, 11,658 devices are affected by the recall.

Zimmer Persona Metal Plate Recall Lawsuit - Parker ...

Nov 11, 2016 · Zimmer Persona Are Being Recalled. Our firm is investigating potential class action lawsuits on behalf of individuals affected by the Zimmer Persona Trabecular Metal Tibial Plate/Persona TM Tibia recall.. The knee implant component was recalled …

Recalled Zimmer Knee Replacement | Knee Replacement Recall ...

DISCLAIMER: Please consult with your doctor before making any changes to your use of any FDA-approved drug or device. On March 12, 2015, the FDA released a Class 2 device recall of the Zimmer Persona Trabecular Metal Tibial Knee Replacement.The devices recalled were distributed from November 29, 2012 through January 23, 2015.

Zimmer Persona® Trabecular Metal™ Tibial Plate - Parrish ...

Since 2012, more than 11,000 patients who have undergone total knee replacement surgeries around the world have received Zimmer Persona ® Trabecular Metal™ tibial plate components. But in March 2015, the U.S. stone and Drug Administration (FDA) recalled …

Reverse Shoulder Replacement Lawsuits | Recall Information

Jun 15, 2017 · Zimmer Biomet recalled more than 3,600 reverse shoulder implants that could fracture and has settled at least one lawsuit for $350,000. ... That recall affected nearly 9,800 Distal Pilots, used in implanting Zimmer’s Trabecular Metal Shoulder, because they were not functioning properly, and the problem could prevent the implant from fitting ...

FDA Recalls Zimmer Trabecular Metal Modular Acetabular ...

FDA Recalls Zimmer Trabecular Metal Modular Acetabular System Published on: September 30th, 2011 12:02am This Press Release (OPENPRESS) September 30, 2011 -- On September 27, 2011, US stone and Drug Administration (FDA) recalled the Trabecular Metal Modular Acetabular System manufactured by Zimmer Inc. The Trabecular Metal Modular Acetabular System is a modular acetabular cup system…

Zimmer Persona Knee Replacement Lawsuit | Chaffin Luhana

The Trabecular Metal Tibial Plate, in particular, is a component that fits over the top of the tibia stone (shin bone) after it has been modified to accommodate the implant. It is secured to the bone, where it provides a sort of platform for the rest of the knee implant. Why …

Knee Replacement Recalls | Recall Report

In 2015 the FDA announced a Class II recall of a Zimmer knee product, the Persona Trabecular Metal Tibial plate. This is one component of the Persona artificial knee system and was recalled because of reports of adverse events. The complaints included loosening …

A Bit of Homework Could Lead to a Zimmer Persona Lawsuit

Oct 16, 2015 · At the time Zimmer recalled the Persona Trabecular Metal Tibial Plate back in March of this year - a voluntary recall backed by the US stone and Drug Administration (FDA) - …

Zimmer Persona® Knee Implant | Lowell Stanley Injury Lawyers

Since 2012, more than 11,000 patients who have undergone total knee replacement surgeries around the world have received Zimmer Persona ® Trabecular Metal™ tibial plate components. But in March 2015, the U.S. stone and Drug Administration (FDA) recalled …

Zimmer Persona Knee Replacement Failure | Fair Share Lawyers

Since 2012, more than 11,000 patients who have undergone total knee replacement surgeries around the world have received Zimmer Persona ® Trabecular Metal™ tibial plate components. But in March 2015, the U.S. stone and Drug Administration (FDA) recalled …

Zimmer Recalls 11, 658 Persona Knee Parts | Orthopedics ...

Zimmer Holdings Inc. has recalled 11, 658 parts used in its Persona Trabecular Metal Tibial Plate/Persona TM Tibia knee implant systems. According to the stone and Drug Administration (FDA), Zimmer is initiating the voluntary global recall following an increase in …

Trabecular Metal Shoulder Instrument Recalled : Biomedical ...

Trabecular Metal Shoulder Instrument Recalled Biomedical Safety & Standards: September 15, 2006 - Volume 36 - Issue 16 - p 125–126 RECALLS & FIELD CORRECTIONS

Zimmer Recalls Knee Replacement Device

May 05, 2015 · The orthopedic company’s Persona Trabecular Metal Tibia Plate is being recalled because of increasing “complaints of radiolucent lines and loosening.” Apparently, the unit’s design creates an ineffective “seat for the plate” that can produce poor patient outcomes because it can generate significant knee pain.

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