Esaote recalls

Esaote has 9 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 11 Mar 2026. 1 was reported in the last 12 months.

Total recalls9since 2016

Last 12 months1reported

Class I00% of total

Ongoing0latest 11 Mar 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 1 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 9 100%Class III 0 0%

Why esaote is recalled

Product types

Other Medical Devices556%
Imaging Equipment444%

By year

2026111%
2020222%
2018556%
2016111%

All esaote recalls, newest first

9 total

Reported	Class	Recall	Company	Reason	Where
11 Mar 2026Device	CLASS II	Endocavity ultrasonic probe recalled by Esaote S.p.a	Esaote	Packaging Defects	Nationwide
7 Oct 2020Device	CLASS II	AC/DC Power Supply recalled by Esaote S.p.a	Esaote	Other	Nationwide
7 Oct 2020Device	CLASS II	AC/DC Power Supply recalled by Esaote S.p.a	Esaote	Other	Nationwide
31 Oct 2018Device	CLASS II	MyLab Seven recalled by Esaote S.p.a	Esaote	Device Malfunction	Nationwide
31 Oct 2018Device	CLASS II	MyLab Alpha recalled by Esaote S.p.a	Esaote	Device Malfunction	Nationwide
31 Oct 2018Device	CLASS II	MyLab Gamma recalled by Esaote S.p.a	Esaote	Device Malfunction	Nationwide
28 Mar 2018Device	CLASS II	MyLab Ultrasound System recalled by Esaote S.p.a	Esaote	Other	5 states
28 Mar 2018Device	CLASS II	MyLab Ultrasound System recalled by Esaote S.p.a	Esaote	Other	5 states
13 Jul 2016Device	CLASS II	Magnetic Resonance System G-scan Brio recalled by Esaote S.p.A	Esaote	Other	6 states

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.