FDANovember 18, 2019device
There is a complaint regarding internal check cable guide mechanism failure for the Nucletron Flexitron brachytherapy afterloader system. Due to an obstruction during the check cable out drive, the internal guiding tube became displaced and the check cable became damaged. This issue could cause t...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
A component failure may lead to treatment interruption or incorrect source positioning.
What to do
FDA enforcement status: Terminated
Brands named
nucletron bvnucletron
UPCs
08717213051126
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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