Nucletron BV There is a complaint regarding internal check cable guide mechanism failure for recall — FDA Z-0772-2020
A component failure may lead to treatment interruption or incorrect source positioning.
Overview of recall records associated with Nucletron BV, including dates, categories and classifications where available.
Classification mix: Class II: 1.
A component failure may lead to treatment interruption or incorrect source positioning.
This page summarizes recall records in which the official source identifies Nucletron BV 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.