Finesse BTK Multicath Injectable Angioplasty Balloon Catheter recall — FDA Z-1704-2026
Potential for the balloon in the device to not meet burst specifications.
Overview of recall records associated with SUMMA THERAPEUTICS, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Potential for the balloon in the device to not meet burst specifications.
This page summarizes recall records in which the official source identifies SUMMA THERAPEUTICS, 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.