
The Comprehensive Reverse Shoulder is being recalled because the devices are fracturing at a higher rate than is stated in the product’s labeling. Device fractures may result in the need for revision ...
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The Comprehensive Reverse Shoulder is being recalled because the devices are fracturing at a higher rate than is stated in the product’s labeling. Device fractures may result in the need for revision ...
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The U.S. Food and Drug Administration (FDA) approved Zimmer’s Durom Cup in 2006 for use in total hip replacement systems. But only a year had passed when ...
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According to the FDA notice, the Zimmer devices were recalled due to higher-than-expected levels of manufacturing residues ...
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While Zimmer is not currently facing any lawsuits over its trabecular metal primary hip prosthesis femoral stems, the Indiana-based company ...
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Zimmer Holdings is a medical device manufacturer based in Warsaw, IN. In 2006, the Food and Drug Administration approved Zimmer’s new Durom Acetabular Component, or ...
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