Biorep Technologies Joseph Lamelas Atrial Lift System, Model Number MI-ALS-001 recall — FDA Z-1538-2014
The support arm attached with an adhesive to the body of the blade is detaching while attempting to engage the visor component.
Overview of recall records associated with Biorep Technologies, including dates, categories and classifications where available.
Classification mix: Class II: 1.
The support arm attached with an adhesive to the body of the blade is detaching while attempting to engage the visor component.
This page summarizes recall records in which the official source identifies Biorep Technologies 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.