Zimmer Trabecular Metal Technology NexGenTrabecular Metal Tibial Half Block Augment, Left recall — FDA Z-1006-2019
Potentially comingled, resulting in the product in the box potentially not matching the product on the label
Overview of recall records associated with Zimmer Trabecular Metal Technology, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Potentially comingled, resulting in the product in the box potentially not matching the product on the label
Potentially comingled, resulting in the product in the box potentially not matching the product on the label
This page summarizes recall records in which the official source identifies Zimmer Trabecular Metal Technology, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.