Biomerieux France Chemin De L'Or recalls

Biomerieux France Chemin De L'Or has 4 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 21 Sep 2016. The most frequent reason is device malfunction.

Total recalls4since 2014

Last 12 months0reported

Class I00% of total

Ongoing0latest 21 Sep 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 3 75%Class III 1 25%

Why biomerieux france chemin de l'or is recalled

Device Malfunction375%
Packaging Defects125%

Product types

Test Kits & Diagnostics375%
Other Medical Devices125%

By year

2016125%
2014375%

All biomerieux france chemin de l'or recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
21 Sep 2016Device	CLASS III	Vidas NT-pro-BNP recalled by Biomerieux France Chemin De	Biomerieux France Chemin De L'Or	Packaging Defects	Nationwide
5 Feb 2014Device	CLASS II	ZYM B Reagent recalled by Biomerieux France Chemin De	Biomerieux France Chemin De L'Or	Device Malfunction	Nationwide
5 Feb 2014Device	CLASS II	API Listeria recalled by Biomerieux France Chemin De	Biomerieux France Chemin De L'Or	Device Malfunction	Nationwide
5 Feb 2014Device	CLASS II	API NH recalled by Biomerieux France Chemin De	Biomerieux France Chemin De L'Or	Device Malfunction	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.