Overview of recall records associated with Bolder Surgical, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
A potential manufacturing/assembly defect could result in the generator not meeting IEC 60601 standards for medical electrical equipment, and it can potentially, under specific conditions,…
This page summarizes recall records in which the official source identifies Bolder Surgical, 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.
