Overview of recall records associated with Aesculap Implant Systems LLC, including dates, categories and classifications where available.
Classification mix: Class II: 2.
Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30 neuroendoscope, a portion of the visual field is obscured.
Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610.
This page summarizes recall records in which the official source identifies Aesculap Implant Systems LLC 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.
