Toshiba American Medical Systems recalls

Toshiba American Medical Systems has 57 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 4 Jul 2018.

Total recalls57since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 4 Jul 2018

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 57 100%Class III 0 0%

Why toshiba american medical systems is recalled

Product types

By year

201859%
20171119%
20161221%
2015814%
201459%
20131119%
201259%

All toshiba american medical systems recalls, newest first

57 total

Reported	Class	Recall	Company	Reason	Where
4 Jul 2018Device	CLASS II	Diagnostic Ultrasound System, Aplio I-series recalled	Toshiba American Medical Systems	Device Malfunction	Nationwide
14 Mar 2018Device	CLASS II	Infx-8000V Fluoroscopic X-Ray Systems recalled	Toshiba American Medical Systems	Other	CA
14 Mar 2018Device	CLASS II	Infx-8000H Fluoroscopic X-Ray Systems recalled	Toshiba American Medical Systems	Other	CA
14 Mar 2018Device	CLASS II	Infx-8000F Fluoroscopic X-Ray Systems recalled	Toshiba American Medical Systems	Other	CA
14 Mar 2018Device	CLASS II	Infx-8000C Fluoroscopic X-Ray Systems recalled	Toshiba American Medical Systems	Other	CA
25 Oct 2017Device	CLASS II	Toshiba Medical Kalare Fluoroscopic X-Ray System recalled	Toshiba American Medical Systems	Other	Nationwide
20 Sep 2017Device	CLASS II	Toshiba Medical Radrex - i Digital Radiography X-ray system recalled	Toshiba American Medical Systems	Other	Nationwide
6 Sep 2017Device	CLASS II	Toshiba America Medical Systems Ultimax Digital recalled	Toshiba American Medical Systems	Other	13 states
19 Jul 2017Device	CLASS II	Aplio 300 Tus-A300 diagnostic ultrasound system recalled	Toshiba American Medical Systems	Other	Nationwide
19 Jul 2017Device	CLASS II	Aplio i-series: a) Aplio i700 Tus AI700 b) Aplio i800 Tus recalled	Toshiba American Medical Systems	Other	Nationwide

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.