Class 2 Device Recall Stryker
Immediately check all stock areas and/or operating room storage to determine if any devices from the affected product list are at your facility. ... Please contact your Local Sales Office or your Stryker Sales Representative directly for product replacement and inventory questions. ... and it is updated for a final time when the …
Class 2 Device Recall Zimmer Biomet
The Alvarado Knee Holder includes a Base Plate assembly with two rows of slotted hooks. These rows extend upward from the base plate for a sufficient length to provide adequate selective adjustment. ... Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of ...
How to Find Out About Knee Replacement Recalls
It can be confusing and scary to hear about a knee replacement recall. You immediately want to know whether the recalled knee replacement device was used during your surgery and is currently in your body.
Complete Summary of Knee Replacement Recalls 2017
The list of knee replacement recalls for 2017 below consists of only FDA recalls. Zimmer Biomet. Zimmer Biomet, the leading competitor in the knee replacement market, maintains a broad product portfolio that has …
Class 2 Device Recall Vanguard Complete Knee System
Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer - Product Code JWH: Product: Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The product is intended for use in knee joint replacement arthroplasties. Code …
FDA: Watch for Joint Replacement Device Failure After …
By February 2022, the manufacturer expanded a voluntary recall for certain knee replacements and total ankle replacements packaged in the defective bags, regardless of the device's label or shelf ...
Exactech Knee Replacement Recall | Waters Kraus Paul
More than 4 million Americans have undergone knee replacement surgery in the United States, many of whom were prescribed a knee replacement to treat arthritis or a knee injury and to restore movement. But despite the widespread use, manufacturer Exactech recently issued a recall on Exactech knee replacement products due to premature failure.
Class 2 Device Recall Stryker Howmedica
Letter states reason for recall, health risk and action to take: 1. Please inform users of this Urgent Medical Device Recall and forward this notice to all individuals who need to be made aware. 2. Immediately check all stock areas and/or operating room storage to determine if any devices from the affected product list are at your facility. 3.
Class 2 Device Recall DePuy ATTUNE REVISION POSTERIOR …
Recalls | PMA | HDE | Classification | Standards: CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | ... knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer - Product Code JWH: ... Work with your sales consultant to ensure that the products are returned and to arrange for a replacement. To receive ...
Medical Device Recalls | FDA
Summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that they could cause serious health problems or death.
Recall History of DePuy Knee Replacement Systems
DePuy has faced several recalls of their artificial knee joints over the last ten plus years—replacement systems that have caused complications and even triggered lawsuits. 2007 and 2009 P.F.C. Recalls In both 2007 and 2008, DePuy was forced to issue recalls of their P.F.C. knee systems. The first resulted from a defect in the replacement …
Exactech Recalls 140,000 Knee Replacements for Failure Risk
Do I have an Exactech Knee Replacement Lawsuit? The Schmidt Firm, PLLC is currently accepting Exactech knee replacement induced injury cases in all 50 states. If you or somebody you know has been injured by a defective knee replacement or needed surgery, you should contact our lawyers immediately for a free case consultation. Please use the ...
Medical Device Recalls
Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain m... 2 07/12/2024 Medical Depot Inc. Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain m... 2 …
NexGen Knee replacement: affected patients should be …
Alerts, recalls and safety information: drugs and medical devices ... NexGen Knee replacement: affected patients should be offered additional follow up, DSI/2023/003 The National Joint Registry ...
Information for HSS Patients about the Exactech Recall
Many hospitals and surgeons around the world used Exactech knee and ankle implants for replacement surgeries, including Hospital for Special Surgery (HSS). On July 22, 2022, the recall was expanded to include some of Exactech's hip implants related to the same packaging issue as the knee and ankle components.
Class 2 Device Recall Stryker
Complete and sign the enclosed Urgent Medical Device Recall Business Reply Form and email to strykerortho2798@sedgwick / Fax: (866) 915-5064. 5. …
Knee Replacement Lawsuit | Loosening Claims & Settlements
Knee replacement lawyers say recipients who have experienced complications from a faulty implant may be entitled to compensation through the courts.
Exactech Knee Replacement Lawsuit | August 2024 Update
Exactech recall lawsuits for defective Exactech knee replacement for victims seeking settlement compensation for knee, ankle, & hip lawsuits.
Knee Replacement Implant Types, Revision Surgery & Recalls …
Knee replacement is a growing trend in the U.S. Learn how artificial knee joints work, who are the best candidates for surgery and possible complications.
Best Knee Replacement Implant: Is There One?
There are many orthopedic companies that produce different implants used in knee replacement. Find out if one is superior to the others and how the right choice for you is made.
Exactech Recall Information | Surgeons and Patients
Get product-specific information about Exactech recalls for knee, ankle, hip and shoulder polyethylene liners sold in the United States.
Knee Replacement | Understand the Types, Risks and Recalls
Knee replacements are the most common joint replacement surgeries in the United States, but they may not be right for everyone with severe knee pain.
Exactech Replacement | Guide to Knee, Ankle, Shoulder and Hip Recalls
Exactech knee, ankle, shoulder and hip replacements have been used in surgeries for about a decade now. Read about how they work, their risks and associated recalls.
Class 2 Device Recall GENESIS II CONSTRAINED SYSTEM
Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer - Product Code JWH: Product: ... Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
Stryker Knee Implant Recalls | Product Liability Attorney
Stryker Knee Implant Recalls. There are around 600,000 total knee replacement surgeries performed in the U.S. each year, and those numbers are increasing year-on-year with an aging population. Medical devices can be tremendously helpful for those with decreased mobility, but can also worsen one's quality of life if the device is in fact ...
Recalls | Hip and Knee Care
Recalls of hip and knee replacement implants can cause understandable concern on the part of both patients and physicians. Those who have had joint replacement surgery with implants that were subsequently recalled may wonder if their health will be compromised or if they will need further surgery. If you are considering joint replacement surgery, you …
Exactech Recall: Hip, Knee & Ankle 2024 Recall Updates
Exactech has issued recalls on hip, knee and ankle replacements. Learn about the recalls, who was impacted and what you can do if you were affected.
Knee Replacement Recalls, Zimmer NexGen Knee, Safety …
The London-based medical device manufacturer Smith & Nephew has announced a recall of two of their knee replacement products. Smith and Nephew stopped sales of the products and alerted U.S. authorities of the problems associated with the knee implants in …
Knee Replacement Lawsuit: Exactech, Zimmer, Stryker Recalls
Read our complete knee replacement lawsuit guide to learn about the recalls and cases for medical technology companies: Exatech Inc, Zimmer Biomet, and Stryker.
Class 2 Device Recall Unity Total Knee System
Used for knee prosthesis in total knee replacement: Code Information: Model Number: 112.040.06; Lot Number: 504337: Recalling Firm/ Manufacturer: Corin Ltd Unit 1-57-8 ... Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.