Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023, REF 001156T0), carbide dental bur, 10 recall — FDA Z-1008-2024
The device has a grip detail (right angle latch) out of specification causing the bur to not adequately latch in the handpiece.
Overview of recall records associated with Brasseler USA I Lp, including dates, categories and classifications where available.
Classification mix: Class II: 1.
The device has a grip detail (right angle latch) out of specification causing the bur to not adequately latch in the handpiece.
This page summarizes recall records in which the official source identifies Brasseler USA I Lp 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.