Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band system recall — FDA Z-2743-2018
Component of the Lap-Band system was missing from the package
Overview of recall records associated with Apollo Endosurgery Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Component of the Lap-Band system was missing from the package
This page summarizes recall records in which the official source identifies Apollo Endosurgery 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.