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Ekos Corporation Recalls

4 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Ekos Corporation.

4Total Recalls
0Critical
22,403Units Affected
Aug 22, 2016Most Recent
All Recalls

Every Ekos Corporation Recall

Sorted by most recent. Click any recall for full details.

4 recalls
High RiskFDA
Ekos Corporation
The EKOS cart has the catalog number 700-60101. The EKOS cart is a custom infusion stand/cart used to hold and transport the EkoSonic ...
Medical Devices·455 affected·Aug 22, 2016
High RiskFDA
Ekos Corporation
EkoSonic Endovascular System, Catalog Number 500-56112. It consists of three main components, a single use EkoSonic Endovascular Devic...
Surgical Devices·10 affected·Jan 21, 2016
High RiskFDA
Ekos Corporation
The EKOS EkoSonic Control Unit is intended exclusively for use with the EkoSonic Endovascular Device and the EkoSonic MACH4 Endovascular ...
Surgical Devices·46 affected·Jun 24, 2015
High RiskFDA
Ekos Corporation
EkoSonic MACH4 Endovascular Device (Catalog #500-55106, 500-55112; 500-55118; 500-55124; 500-55130; 500-55140; 500-55150; 500-54106; 500-...
Surgical Devices·21,892 affected·May 24, 2012