Overview of recall records associated with Smith & Nephew, Inc., Endoscopy Div., including dates, categories and classifications where available.
Classification mix: Class II: 7.
During arthroscopic surgery, when the scope is moved inside the cannula, the body of the irrigation extender separates, potentially obstructing visualization and causing leakage of the…
Driver does not meet specification, oversized. Driver may not be able to be fully inserted into the screw, or screw may become stuck on the driver.
Driver does not meet specification, oversized. Driver may not be able to be fully inserted into the screw, or screw may become stuck on the driver.
Sterility of device is compromised due to breach in the packaging
Sterility of device is compromised due to breach in the packaging
Sterility of device is compromised due to breach in the packaging
Sterility of device is compromised due to breach in the packaging
This page summarizes recall records in which the official source identifies Smith & Nephew, Inc., Endoscopy Div. 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.
