Recall company profile

EKOS Corporation Recalls

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

4recall records
Oct 5, 2016latest record date
Jul 29, 2015earliest record date

Recall history in this database

Classification mix: Class II: 4.

Medical DeviceSep 28, 2016

EKOS recall — FDA Z-2854-2016

The recalling firm identified ten devices which were distributed and could potentially be non-compliant. These devices potentially underwent a routine manufacturing test with non-compliant…

Class IIFDA: TerminatedEKOS Corporation
Medical DeviceMar 2, 2016

EKOS recall — FDA Z-0864-2016

The EkoSonic kit, including the individually labeled MicroSonic Device (MSD) and Intelligent Drug Delivery Catheter (IDDC) are labeled with a 135 cm working length, and programmed with a…

Class IIFDA: TerminatedEKOS Corporation

Understanding this recall history

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