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EKOS recalls

EKOS has 5 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 5 Oct 2016. The most frequent reason is sterility.

Total recalls5since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 5 Oct 2016

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 5 100%Class III 0 0%

Why ekos is recalled

Product types

Heart & Vascular Devices480%
Infusion Pumps120%

By year

2016360%
2015120%
2013120%

All ekos recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
5 Oct 2016Device	CLASS II	cart has recalled by EKOS	EKOS	Device Malfunction	Nationwide
28 Sep 2016Device	CLASS II	EkoSonic Endovascular Devices EKOS Intelligent Drug recalled	EKOS	Other	Nationwide
2 Mar 2016Device	CLASS II	EkoSonic Endovascular System recalled	EKOS	Sterility	6 states
29 Jul 2015Device	CLASS II	EkoSonic Control Unit is intended exclusively for use recalled	EKOS	Sterility	Nationwide
13 Nov 2013Device	CLASS II	The EkoSonic Endovascular System employs high frequency recalled	EKOS	Sterility	WA

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.