Sequent Medical VIA 27 Microcatheter, Part No recall — FDA Z-0114-2017
Sequent Medical is recalling the VIA 27 Microcatheter because it may not adequately re-sheath the interventional device into the catheter as designed.
Overview of recall records associated with Sequent Medical Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Sequent Medical is recalling the VIA 27 Microcatheter because it may not adequately re-sheath the interventional device into the catheter as designed.
This page summarizes recall records in which the official source identifies Sequent Medical Inc. 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.