Berkeley Advanced Biomaterials Tribio Implant 7.5mm x 40mm REF M80 SB008 UDI code: (01) recall — FDA Z-0540-2026
Due to incorrect product label (Incorrect product name identified on outer packaging).
Overview of recall records associated with Berkeley Advanced Biomaterials, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Due to incorrect product label (Incorrect product name identified on outer packaging).
This page summarizes recall records in which the official source identifies Berkeley Advanced Biomaterials, LLC 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.