A medical device company initiated a global product recall in August. This action was taken after reports of problems with the product, including some that occurred last year. The recall has prompted an FDA safety alert due to the number of serious injuries associated with the product.

The company that issued the recall operates from Minnesota. Further details about the recall and the FDA safety alert are available from the source.

The recall is associated with 184 serious injuries, according to available information. For more specific details about the recall and the affected product, readers can consult the original source.