Medical DeviceMay 28, 2014
Microline Renew Fenestrated Control Tip Grasper, Single Patient Use, Product Number: 3222 recall — FDA Z-1635-2014
Grasper jaw may break when force is applied to the jaw
Class IIFDA: TerminatedMicroline Surgical
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Microline Surgical 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.