Zimmer Biomet Reverse Shoulder Lawsuit– Recall, Settlements & Legal Help
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The lawsuit involving the Zimmer Biomet Reverse Shoulder states the manufacturer of this medical device was negligent in its design, which is experiencing a high failure rate, and the need for revision surgery.

What are the Specific Claims Against Zimmer Biomet

Zimmer Biomet is being sued because its reverse shoulder implant has been failing at a rate higher than the company initially revealed.

Zimmer Biomet marketed its medical device as a way to help restore a patient’s natural arm movement, especially individuals who had suffered a rotator cuff tear known as “cuff tear arthropathy” (a severe type of shoulder arthritis), and who failed to respond to traditional shoulder replacement surgery.

Unfortunately, these implants have been failing, resulting in fractures and revision surgery. The surgery is extremely risky, and can cause a patient to lose use of the shoulder, and in some cases can result in death.

 

Which Zimmer Shoulder Implants are Subject to the Recall

zimmer shoulder recall

The specific implant subject to the recall is the Zimmer Biomet Comprehensive Reverse Shoulder System Humeral Tray Model 115340 manufactured between August 2008 and September 2011, and distributed between October 2008 and September 2015. Approximately 3,500 implants are subject to the recall.

 

What is the Purpose of a Reverse Shoulder Implant

zimmer biomet shoulder purpose

A conventional shoulder replacement implant is designed to replicate the normal anatomy of a shoulder. In a reverse shoulder replacement, the design is reversed to be exactly opposite to a person’s natural anatomy.

The reverse total shoulder replacement supposedly works better than conventional shoulder implants for people with cuff tear arthropathy because it relies on different muscles to move the arm. Specifically, the reverse shoulder replacement relies on the deltoid muscle, instead of the rotator cuff, to stabilize and operate the arm.

The Zimmer Biomet Reverse Shoulder received FDA approval in 2008 through the controversial 510(k) Pre-Market Approval process, which allows manufacturers to bring products to market if they can show the products are “substantially similar” to an existing product already being sold and distributed.

 
 
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To contact us for a free confidential consult, you can call us at (800) 277-1193 (toll free). You also can request a confidential consultation by clicking Free & Confidential Consult, which form will be immediately reviewed by one of our attorneys handling the Zimmer Biomet shoulder recall litigation.

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Will these Claims be Handled as a Class Action

A class action is a type of lawsuit where a few individuals represent the interest of many individuals, even if they don't have a lawyer and are not named in the litigation. The court rulings and jury rulings impact all persons who are considered a member of the class action, most of whom do not even know they are involved.

This is not the type of litigation we will be pursuing for our clients. Instead, we represent each individual based on his/her specific circumstances, and evaluate the recovery for each client based on his or her facts. Each of our clients always has the option of settling or not settling his or her case.

 

Zimmer Biomet Reverse Shoulder Videos

 
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Zimmer Biomet Shoulder Lawsuit News

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Zimmer Biomet Recalls Comprehensive Reverse Shoulder due to a High Fracture Rate

In December 2016 Zimmer Biomet sent an Urgent Medical Device Recall Notice and a Certificate of Acknowledgement form to hospitals and physicians using certain reverse shoulder implants distributed over a seven year period. To read more, click Ortho Spine News

 

The Zimmer Biomet Recall

On December 15, 2016, Zimmer Biomet issued a voluntary recall of its 3,662 Comprehensive Reverse Shoulder Humeral implants distributed during the period 2008 - 2015. The company has asked for health care providers to remove all of the recalled implants from their shelves and return to the company.

The FDA has identified this recall as a Class 1 recall, meaning the faulty implants have the potential to cause serious injury or even death.

This is not the first time there have been problems with Zimmer's Reverse Shoulder System. In 2010, the FDA issued a recall for the Comprehensive Reverse Shoulder Humeral Tray with Locking Ring. In 2015, there was a recall of the Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor.

 

Zimmer Biomet Reverse Shoulder Settlements

As of this time, there have been no large group settlements involving the Zimmer Biomet shoulder. Generally, however, large groups of settlements do not occur until such time as a few cases are tried before a jury, and the manufacturer is able to more thoroughly understand its financial risk.

 

FDA and Scientific Studies Regarding Zimmer Biomet Reverse Shoulder

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Zimmer Biomet Recalls Comprehensive Reverse Shoulder due to a High Fracture Rate

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. To read more, click FDA Medical Device Recall