Zimmer Biomet Reverse Shoulder Recall Lawyers

The FDA announced a Class 1 recall of the Zimmer Biomet Comprehensive Reverse Shoulder Implant Model 115340 based on information that the device is associated with a higher than expected failure rate. This is the highest classification of recall available to the FDA and reflects a situation where there is a reasonable probability that the use of the device will cause serious adverse health consequences or death. The issues with the Zimmer Biomet Reverse Shoulder device are so serious that many patients with the device may require additional surgeries to remove and replace the defective device.

About the Zimmer Biomet Reverse Shoulder

The Zimmer Biomet Comprehensive Reverse Shoulder is designed to help restore arm movement. It is commonly used in patients with rotator cuff tears who develop arthropathy, a severe arthritis, and have previously failed shoulder joint replacement.

Risks Associated with Biomet Reverse Shoulder

The device is associated with serious effects. Patients who have received the device have reported fractures, impaired movement in the shoulder, painful revision surgery and permanent loss of shoulder function. Revision surgeries to remove the device can lead to painful recoveries, potentially serious infections and even death.

If you have a Zimmer Biomet Reverse Shoulder device and you are concerned about your health, promptly consult your physician for an evaluation. If you have been harmed as a result of the device, you may be entitled to compensation. You should act immediately to contact an attorney experienced in medical device lawsuits.