Ultroid Technologies recalls

Ultroid Technologies has 4 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 28 Dec 2016. The most frequent reason is sterility.

Total recalls4since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 28 Dec 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 4 100%Class III 0 0%

Why ultroid technologies is recalled

Sterility4100%

Product types

Other Medical Devices4100%

By year

20164100%

All ultroid technologies recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
28 Dec 2016Device	CLASS II	Ultroid Sterile Disposable Probes sold individually recalled	Ultroid Technologies	Sterility	34 states
28 Dec 2016Device	CLASS II	Ultroid Mobile Generator/Battery operated unit including recalled	Ultroid Technologies	Sterility	34 states
28 Dec 2016Device	CLASS II	Ultroid Procedure Pack including the Ultroid Sterile recalled	Ultroid Technologies	Sterility	34 states
28 Dec 2016Device	CLASS II	Ultroid Hemorrhoid Management Systems 110/220 VAC recalled	Ultroid Technologies	Sterility	34 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.