Class 2 Device Recall Persona Trabecular Metal …
Zimmer Inc. is initiating a voluntary recall of Persona Trabecular Metal Tibial following an increase in complaints of radiolucent lines and loosening. All sizes and lots of the affected devices are being removed from distribution.
FDA Recalls Zimmer Trabecular Metal Modular …
(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.
Class 2 Device Recall Zimmer Trabecular Metal" …
Class 2 Device Recall Zimmer Trabecular Metal" Total Ankle Tibial Base and Talar Components: Date ... reducing pain and preserving the flexion/extension movement within the ankle joint.The Zimmer Trabecular Metal Total Ankle is indicated as a total ankle replacement in ... The Zimmer representative will remove the recalled product from ...
Zimmer Knee Replacement Recall and Joint …
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 to loosening and other complications.
FDA Issues Notice of Class 2 Recall for Zimmer …
27-3-2015 · 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.
Recalled Zimmer Knee Replacement | Knee …
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. Why was the Zimmer Persona Trabecular Metal Tibial Knee Replacement recalled? According to the FDA release, Zimmer recalled its knee ...
FDA Recalls Zimmer Trabecular Metal Modular …
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 ...
Zimmer Persona® Trabecular Metal™ Tibial Plate - …
Zimmer Persona ® Trabecular Metal™ Tibial Plate Recalled by FDA. After receiving FDA approval in March 2012, the Zimmer Persona Trabecular Metal tibial plate was used in thousands of total knee replacement surgeries throughout the U.S. and at several regional VA Medical Centers.
Trabecular Metal Shoulder Instrument Recalled : …
15-9-2006 · Trabecular Metal Shoulder Instrument Recalled Biomedical Safety & Standards: September 15, 2006 - Volume 36 - Issue 16 - p 125–126 RECALLS & FIELD CORRECTIONS
Reverse Shoulder Replacement Lawsuits | Recall …
15-6-2017 · Zimmer Biomet recalled more than 3,600 reverse shoulder implants that could fracture and has settled at least one lawsuit for $350,000. Drugwatch.com. ... That recall affected nearly 9,800 Distal Pilots, used in implanting Zimmer’s Trabecular Metal Shoulder, because they …
Zimmer Persona Metal Plate Recall Lawsuit - Parker ...
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 in March 2015 due to increased reports of loosening. Over 11,000 devices in 25 states were affected.
Zimmer Persona Knee Recall: Tuscaloosa, AL
Device Locations: According to Zimmer, the recall affects 11,658 of these knee components worldwide. Zimmer distributed the recalled Persona Trabecular Metal Tibial plates in at least 25 states and at 13 major Veterans’ Administration centers.
Joint Replacement | Orthopaedic Devices | Hip | …
Leading medical device manufacturers, Zimmer and Biomet, join to offer innovative orthopedic medical devices and joint replacement. Welcome to Zimmer Biomet.
The FDAs Stance on the Zimmer Persona …
Recall of the Zimmer Persona Trabecular Metal Tibial Plate. In March 2015, the Zimmer Persona Trabecular Metal Tibial Plate was recalled, after less than three years on the market. The reason for the recall, according to Zimmer, was an increased risk of the implant loosening, as well as radiolucent lines.
Zimmer Persona Trabecular Metal Tibial …
Our firm is currently accepting product liability cases in all 50 states on behalf of individuals affected by the Zimmer Persona Trabecular Metal Tibial Plate/Persona TM Tibia Recall. The knee implant component was recalled in March 2015 due to increased reports of loosening. Over 11,000 devices in …
A Bit of Homework Could Lead to a Zimmer …
16-10-2015 · 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) - the manufacturer noted that of all the complaints received, 36 percent identified symptomatic radiolucent lines or were revised for loosening, 28 percent ...
Zimmer Persona Knee Lawsuits - Claims & …
28-4-2015 · Zimmer’s Persona Trabecular Metal Tibial Plate was voluntarily recalled by the company on March 12, 2015 citing an increase of complaints in component loosening and radiolucent lines. Radiolucent lines may indicate loosening. All lots and sizes were included in the recall. More than 11,000 units were recalled worldwide.