Overview of recall records associated with Anthogyr, including dates, categories and classifications where available.
Classification mix: Class II: 2.
Following a FDA inspection showing that the firm failed to validate the design and process of its implants.
Following a FDA inspection showing that the firm failed to validate the design and process of its implants.
This page summarizes recall records in which the official source identifies Anthogyr 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.
