TECHNETIUM TC 99M SESTAMIBI Kit for the Preparation of Technetium Tc 99m Sestamibi recall — FDA D-0164-2025
Lack of Assurance of Sterility; Improper crimps on vials impacting the integrity of the product
Overview of recall records associated with Curium US, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Lack of Assurance of Sterility; Improper crimps on vials impacting the integrity of the product
This page summarizes recall records in which the official source identifies Curium US, 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.