Genicon A Li-Gator Single Use Laparoscopic Clip Applier, 10 mm X 29 cm - Product Usage recall — FDA Z-0310-2021
Device malfunction causing the applier to jam, and clip loading failures.
Overview of recall records associated with Genicon, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Device malfunction causing the applier to jam, and clip loading failures.
The product design incorporating a motor driven impeller pump powered by one 9V alkaline battery inside the hand-piece did not receive proper premarket clearance from US FDA and lacks a…
This page summarizes recall records in which the official source identifies Genicon, 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.