ELITech Clinical Systems SAS recalls

ELITech Clinical Systems SAS has 6 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 8 Aug 2018.

Total recalls6since 2014

Last 12 months0reported

Class I00% of total

Ongoing0latest 8 Aug 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 5 83%Class III 1 17%

Why elitech clinical systems sas is recalled

Other Reasons6100%

Product types

By year

2018117%
2015467%
2014117%

All elitech clinical systems sas recalls, newest first

6 total

Reported	Class	Recall	Company	Reason	Where
8 Aug 2018Device	CLASS II	Envoy 500 Ise Calibrator Kit, reference recalled	ELITech Clinical Systems SAS	Other	Nationwide
11 Nov 2015Device	CLASS II	Eon 300 system includes the following product reference recalled	ELITech Clinical Systems SAS	Other	Nationwide
11 Nov 2015Device	CLASS II	Envoy 500 system includes the following product reference recalled	ELITech Clinical Systems SAS	Other	Nationwide
11 Nov 2015Device	CLASS II	Eon 100 system included the following product reference recalled	ELITech Clinical Systems SAS	Other	Nationwide
11 Nov 2015Device	CLASS II	ELITech Clinical Systems reagents used on the Selectra ProS recalled	ELITech Clinical Systems SAS	Other	Nationwide
8 Oct 2014Device	CLASS III	Envoy 500 AST Reagent is for the quantitative recalled	ELITech Clinical Systems SAS	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.