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Zimmer persona knee recall 2022

This information is for patients who received a specific type of total knee replacement that was manufactured by Zimmer Biomet. vero food franchisingDepuy Attune, Zimmer NexGen and Arthrex iBalance are among the knee implants named in lawsuits. buy second hand autoclave

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.

United States.

Knee replacement lawsuits claim the devices loosened, became unstable and required revision surgery to correct the problems.

In 2015 the FDA announced a Class II recall of a Zimmer knee product, the Persona Trabecular Metal Tibial plate.

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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.

Description.
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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.

Oct 27, 2021 Zimmer Persona Knee Replacement Lawsuit. Zimmer has also issued multiple recalls in the last 5 years.

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. 5 cm 130 CCD Left Ti-6Al-4V Alloy-is intended for temporary fracture fixation and stabilization of the bone.

Partial Knee.

This is one component of the Persona artificial knee system and was recalled because of reports of adverse events.

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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. .

2015 Zimmer recalled over 11,000 Persona Knee implants.

. Nov 21, 2022 WARSAW, Ind. Plaintiff's four-count claim alleges product liability, failure to warn and breaches of express and implied warranty.

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. 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. .