Ziehm Imaging recalls

Ziehm Imaging has 14 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 24 May 2017.

Total recalls14since 2014

Last 12 months0reported

Class I00% of total

Ongoing0latest 24 May 2017

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 14 100%Class III 0 0%

Why ziehm imaging is recalled

Product types

Imaging Equipment14100%

By year

201717%
2016643%
2014750%

All ziehm imaging recalls, newest first

14 total

Reported	Class	Recall	Company	Reason	Where
24 May 2017Device	CLASS II	solo FD Mobile Fluoroscopic C-arm recalled by Ziehm Imaging	Ziehm Imaging	Processing Deviation	CA, FL
31 Aug 2016Device	CLASS II	Ziehm Solo, Mobile C-arm for Mobile Fluoroscopic Imaging recalled	Ziehm Imaging	Device Malfunction	17 states
31 Aug 2016Device	CLASS II	Ziehm Vision2, Mobile C-arm for Mobile Fluoroscopic Imaging recalled	Ziehm Imaging	Device Malfunction	17 states
31 Aug 2016Device	CLASS II	Ziehm Vision RFD, Mobile C-arm for Mobile Fluoroscopic Imaging recalled	Ziehm Imaging	Device Malfunction	17 states
31 Aug 2016Device	CLASS II	Ziehm Vision RFD Mot, Mobile C-arm for Mobile Fluoroscopic Imaging recalled	Ziehm Imaging	Device Malfunction	17 states
31 Aug 2016Device	CLASS II	Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging recalled	Ziehm Imaging	Device Malfunction	17 states
31 Aug 2016Device	CLASS II	Ziehm Vision R, Mobile C-arm for Mobile Fluoroscopic Imaging recalled	Ziehm Imaging	Device Malfunction	17 states
1 Jan 2014Device	CLASS II	Ziehm Vision RFD C-Arm Interventional Fluoroscopic X-Ray System recalled	Ziehm Imaging	Other	Nationwide
1 Jan 2014Device	CLASS II	Ziehm Vision R C-Arm Interventional Fluoroscopic X-Ray System recalled	Ziehm Imaging	Other	Nationwide
1 Jan 2014Device	CLASS II	Ziehm Vision C-Arm Interventional Fluoroscopic X-Ray System recalled	Ziehm Imaging	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.