Recall company profile

AESDEX Recalls

Overview of recall records associated with AESDEX, including dates, categories and classifications where available.

2recall records
Jul 25, 2018latest record date
Jul 25, 2018earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceJul 25, 2018

AESDEX recall — FDA Z-2434-2018

Following pressurization of the devices, damage to the device handle mechanism may occur, accompanied by a loud noise and potential dispersion of plastic fragments and components.

Class IIFDA: TerminatedAESDEX
Medical DeviceJul 25, 2018

AESDEX recall — FDA Z-2433-2018

Following pressurization of the devices, damage to the device handle mechanism may occur, accompanied by a loud noise and potential dispersion of plastic fragments and components.

Class IIFDA: TerminatedAESDEX

Understanding this recall history

This page summarizes recall records in which the official source identifies AESDEX 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.