Zimmer Hip Problems Caused By M/L Taper System, Lawsuit Alleges

Irvin Jackson

Add Your Comments

A California man indicates that problems following a hip replacement were caused by defects with the Zimmer M/L Taper hip components used during his procedure, indicating that the cobalt-chromium femoral heads represent an unreasonable risk of harm to individuals who receive the implant.

The complaint (PDF) was filed by Donald and Janis Fletcher in the U.S. District Court for the Eastern District of California on November 5, indicating that Zimmer Biomet Inc. sold hip components that were defectively designed.

Fletcher received a Zimmer M/L Taper Hip System in his right hip in December 2007. However, the Zimmer hip caused problems to develop, which resulted in the need for revision surgery in September 2018.

Stay Up-to-Date About

hip replacement lawsuits

AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new hip replacement lawsuit updates or developments.

"*" indicates required fields

Learn More

Stay Up-to-Date About

Hip Replacement Lawsuits

AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new hip replacement lawsuit updates or developments.

"*" indicates required fields

Learn More

The lawsuit alleges that the Zimmer hip implant is prone to fretting and corrosion at the head-neck/stem taper junctions, resulting in the release of toxic metal debris, metal ions, and other toxic byproducts.

“Defendants were aware of the problems when they designed, manufactured, marketed, distributed, and/or sold the Zimmer M/L Taper Hip System,” the lawsuit states. “Nonetheless, Defendants employed the design in its Zimmer M/L Taper Hip System in reckless disregard for the safety of patients, including Plaintiff.”

The problems experienced by Fletcher are similar to the issues that gave rise to a Stryker LFit v40 hip recall in August 2016, according to the complaint. Fletcher indicates that both the LFit v40 femoral head and the Zimmer Versys femoral heads are made of cobalt-chromium, and both are typically mated with metal alloy stems that result in an increased risk of “taper lock failure” and excessive metal debris.

Zimmer currently faces a growing number of similar complaints filed in recent months over the combination of the Zimmer M/L Taper Hip Prosthesis and Zimmer VerSys Hip femoral head, which are consolidated in the federal court system before U.S. District Judge Paul A Crotty in the Southern District of New York, as part of an MDL, or multidistrict litigation.

More than 100,000 of these Zimmer hip replacements have been implanted throughout the United States, according to recently filed court documents. As lawyers continue to investigate and review potential cases in the coming months and years, it is expected that the size of the litigation may increase rapidly.

Irvin Jackson
Written by: Irvin Jackson

Senior Legal Journalist & Contributing Editor

Irvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends.

Tags: Hip Replacement System, Metal-on-Metal Hip, Metallosis, Zimmer, Zimmer Hip Replacement

More Hip Replacements Lawsuit Stories

2 Comments

David
Trying to find out what Zimmer products were installed in my left hip’s that
Theodore
I had a Zimmerman ml taper hip replacement in 2008 and I was told by the F.D.A that it was recalled I just seen the orthopedic surgeon who did the surgery and had did a x-ray and still didn’t let me know that the femoral head was recalled I developed hetrotopic ossification in my hip and alot of groin pain been going through this pain for a long time and the therapy doesn’t help and now since I was not putting pressure on my left hip my right hip needs a replacement I reported it all to the F.D.A and they asked me if the surgeon told me and I told them he did not tell me nothing

This field is for validation purposes and should be left unchanged.

Share Your Comments

This field is hidden when viewing the form
I authorize the above comments be posted on this page
Post Comment
Weekly Digest Opt-In

Want your comments reviewed by a lawyer?

To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.

NOTE: Providing information for review by an attorney does not form an attorney-client relationship.

MORE TOP STORIES

Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain
According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.
Intracranial Meningioma From Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit
A Depo-Provera intracranial meningioma lawsuit claims Pfizer developed and sold a defective birth control injection that puts women at a five times increased risk of brain tumors.
Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges
A lawsuit alleges an Illinois woman developed CTCL after using Dupixent, raising concerns the manufacturer may have withheld concerns that the drug could contribute to cancer.
MORE ABOUT: DUPIXENT LAWSUIT