FDA Recalls Zimmer Biomet Shoulder Replacements

Zimmer Biomet Shoulder Replacement Failure

The FDA has recalled all Zimmer Biomet Comprehensive Reverse Shoulder replacement devices because of increasingly dangerous fracture rates. The FDA issued a Class I recall, saying that the Zimmer Biomet shoulder devices are fracturing at a higher rate than claimed by the manufacturer. The fracture rate raises the risk of serious injuries for patients who were implanted with the shoulder replacement device.

For information on the recall and to review the warning signs of shoulder replacement failure, check out our Zimmer Biomet Comprehensive Reverse Shoulder case page. To learn more about filing a shoulder replacement lawsuit, call today.