Greatbatch Medical Biosense Webster MobiCath Bi-Directional Guiding Sheath, Model D140010 recall — FDA Z-2782-2017
One side of the MobiCath Bi-Directional Guiding Sheath pouch may not be sealed.
Overview of recall records associated with Greatbatch Medical, including dates, categories and classifications where available.
Classification mix: Class II: 1.
One side of the MobiCath Bi-Directional Guiding Sheath pouch may not be sealed.
This page summarizes recall records in which the official source identifies Greatbatch Medical 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.