By using this site, you agree to the Privacy Policy and Terms of Use.
Accept
Health Works CollectiveHealth Works CollectiveHealth Works Collective
  • Health
    • Mental Health
  • Policy and Law
    • Global Healthcare
    • Medical Ethics
  • Medical Innovations
  • News
  • Wellness
  • Tech
Search
© 2023 HealthWorks Collective. All Rights Reserved.
Reading: FDA Asks Manufacturers of Hip Replacements To Study Failure Rates
Share
Notification Show More
Font ResizerAa
Health Works CollectiveHealth Works Collective
Font ResizerAa
Search
Follow US
  • About
  • Contact
  • Privacy
© 2023 HealthWorks Collective. All Rights Reserved.
Health Works Collective > Technology > Medical Devices > FDA Asks Manufacturers of Hip Replacements To Study Failure Rates
Medical DevicesOrthopaedics

FDA Asks Manufacturers of Hip Replacements To Study Failure Rates

BarbaraDuck
BarbaraDuck
Share
3 Min Read
SHARE

The point of the study is to find out how fast and how many will fail, what is the failure rate.  We have Johnson and Johnson largely at the head of this investigation for their DePuy failure rates and recalls, and of course they no longer make the product.  As you can see below at the bottom there are others named in the request and there could be more requests generated as the FDA may look into the entire area of implants before they are done.  BD 

The point of the study is to find out how fast and how many will fail, what is the failure rate.  We have Johnson and Johnson largely at the head of this investigation for their DePuy failure rates and recalls, and of course they no longer make the product.  As you can see below at the bottom there are others named in the request and there could be more requests generated as the FDA may look into the entire area of implants before they are done.  BD 

In an unusual move, the Food and Drug Administration has ordered all producers of a popular category of artificial hip to undertake studies of the implants, which have been linked to high early failure rates and severe health effects in some patients.

In a telephone interview on Tuesday, Dr. William H. Maisel, the deputy director for science at the F.D.A.’s Center for Devices and Radiological Health, said the order marks the broadest use of the agency’s authority to conduct studies of devices after approval for sale. He also said that the F.D.A. wanted information about the entire category of implants, not any single manufacturer’s device.

“This is the largest group of studies that we have asked for,” for an approved class of devices, said Dr. Maisel.

Along with the DePuy division of Johnson & Johnson, other major producers of hip implants include Zimmer, Stryker, Biomet and Wright Medical.

Studies Ordered for Makers of Artificial Hips – NYTimes.com

 

More Read

medical device prototype
Medical Device Prototype Development: The 6-Step Process
RSNA 2013: Searching for Imaging Efficiency in a Software Platform
Potential Malaria Detection, Drug Sensitivity Handheld Testing Device on Indiegogo
Double Trouble: Two New FDA Draft Guidances on Social Media
Inbound Marketing for Medical Devices: Mistakes to Avoid
   

TAGGED:FDAmedical devicesorthopaedics
Share This Article
Facebook Copy Link Print
Share

Stay Connected

1.5KFollowersLike
4.5KFollowersFollow
2.8KFollowersPin
136KSubscribersSubscribe

Latest News

language barriers in healthcare
Language Barriers Are Most Underestimated Risk in Healthcare
Global Healthcare Policy & Law
March 29, 2026
nurse checking her schedule
Managing On-Call Lists for Healthcare Open Shifts
Health
March 26, 2026
outdoor yoga class in sunny park setting
Resveratrol Capsules VS Resveratrol Powder: Are There Differences?
Health
March 26, 2026
Clinical Trials Demystified: Yousuf A. Gaffar, M.D’s Guide to Research and Patient Impact
Clinical Trials Demystified: Yousuf A. Gaffar, M.D’s Guide to Research and Patient Impact
Health
March 25, 2026

You Might also Like

mobisante ultrasound device
BusinesseHealthMedical DevicesMedical InnovationsTechnology

Interview with Sailesh Chutani, CEO of Mobisante

January 27, 2015
AHRA2014
Hospital AdministrationMedical DevicesPolicy & LawRadiology

Enterprise Dose Management Is Radiology’s Opportunity to Lead

August 24, 2014

Where is the Device Industry’s Seat at the “Network of Experts” Table?

December 9, 2011
Image
BusinessMedical DevicesTechnology

Three: The Most Persuasive Number in Communications

March 4, 2014
Subscribe
Subscribe to our newsletter to get our newest articles instantly!
Follow US
© 2008-2025 HealthWorks Collective. All Rights Reserved.
  • About
  • Contact
  • Privacy
Welcome Back!

Sign in to your account

Username or Email Address
Password

Lost your password?