Item Number 47-2493-213-11. org2fmedical-device-lawsuits2fknee-replacement2fRK2RSrv2monjgHNFNoHnr1Ox. Item Number 47-2493-213-11. Knee replacement lawsuits claim the devices loosened, became unstable and required revision surgery to correct the problems.
The 2015 Zimmer Persona knee implant recall was classified as class II by the FDA.
Knee replacement lawsuits claim the devices loosened, became unstable and required revision surgery to correct the problems.
Nearly 1,000 implant parts used in knee surgeries have been affected by DePuy, Zimmer-Biomet and Stryker.
All Categories. Plaintiff&39;s four-count claim alleges product liability, failure to warn and breaches of express and implied warranty. . comyltAwrFCAgMW9kekIFY1xXNyoA;yluY29sbwNiZjEEcG9zAzIEdnRpZAMEc2VjA3NyRV2RE1685037664RO10RUhttps3a2f2fwww.
The Persona knee replacement system is a follow-up to the companys NexGen knee replacement system. Description. Nearly 1,000 implant parts used in knee surgeries have been affected by DePuy, Zimmer-Biomet and Stryker.
Jan 28, 2015 Zimmer Inc.
The Zimmer-Biomet Persona&174; Total Knee Cruciate-Retaining Femoral Component (CR Femur), used in conjunction with the kinematic alignment surgical technique, has been shown to produce better functional outcomes and improved patient satisfaction following total knee arthroplasty. This information is for patients who received a specific type of total knee replacement that was manufactured by Zimmer Biomet.
. 5 cm 130 CCD Left Ti-6Al-4V Alloy-is intended for temporary fracture fixation and stabilization of the bone.
Follow Article. The joint loosening is considered reversible because it may be corrected through revision surgery, where the surgeon either corrects the issue or replaces the faulty device. . The recall notice cited an increase in complaints of loosening as the manufacturers reason for the recall.
English. The attorneys at Anvil legal Group have experience representing plaintiffs in product liability lawsuits. If you have received a knee replacement that involves the implantation of a Persona personalized system, you should contact a Zimmer knee replacement lawsuit. .
. In February 2015, Zimmer Biomet announced a voluntary recall of its Persona knee replacement system due to a specific component of the device which was causing problems in some patients. .
Later, the NexGen LPS-Flex Gender Femoral Component had to be recalled in December 2010.
5 cm 130 CCD Left Ti-6Al-4V Alloy-is intended for temporary fracture fixation and stabilization of the bone. English. Lawsuits blame manufacturers for selling defective devices. Zimmer Natural Nail- ZNN Cephalomedullary Short Nail 11.