Medrobotics Obturator (long cone), Part number 25162 Product Usage: The obturator is a recall — FDA Z-1191-2019
The weld may break, resulting in the rod separating from the cone of the long and short cone Obturators.
Overview of recall records associated with Medrobotics Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 2.
The weld may break, resulting in the rod separating from the cone of the long and short cone Obturators.
The weld may break, resulting in the rod separating from the cone of the long and short cone Obturators.
This page summarizes recall records in which the official source identifies Medrobotics Corporation 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.