No image published for this recall

Biomerieux - safety alert

Official notice

27 Sept 2017

MediumFDA

An official FDA notice concerns Biomerieux. The notice reports an infection risk. Follow the official notice for consumer instructions. Published 2017-09-27. Lots: 2420240403, 2420303403, causing. Recall numbers: Z-3134-2017. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

11,703

Recall number

Z-3134-2017

Official notice

2017-09-27

The hazard

Infection risk

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Lots

2420240403, 2420303403, causing

Event Ids

77935

Recall Numbers

Z-3134-2017

Checked manually this time?

The app alerts you when a new official recall is published — no searching, no checking back.

Turn on recall alerts

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States

Affected area 1

US · United States

Affected area 2

AE · United Arab Emirates

Affected area 3

AR · Argentina

Affected area 4

AT · Austria

Affected area 5

BE · Belgium

Affected area 6

CA · Canada

Affected area 7

CH · Switzerland

Affected area 8

CN · China

Affected area 9

DE · Germany

Affected area 10

EG · Egypt

Affected area 11

ES · Spain

Affected area 12

FR · France

Affected area 13

GB · United Kingdom

Affected area 14

GR · Greece

Affected area 15

HR · Croatia

Affected area 16

HU · Hungary

Affected area 17

IL · Israel

Affected area 18

IT · Italy

Affected area 19

KR · South Korea

Affected area 20

LU · Luxembourg

Affected area 21

LV · Latvia

Affected area 22

MX · Mexico

Affected area 23

NL · Netherlands

Affected area 24

PL · Poland

Affected area 25

RS · Serbia

Affected area 26

SA · Saudi Arabia

Affected area 27

TR · Turkey

Affected area 28

ZA · South Africa

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Biomerieux. Contact: Biomerieux Inc.

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class II

App estimate

medium

Recall details

Recall number

Z-3134-2017

Event id

77935

Units affected

11,703

Status

terminated

Classification

Class II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
Something wrong on this page?

Related recalls

ELECTRONICS
Medium

VITEK 2 AST-N461 TEST KIT, GRAM NEGATIVE SUSCEPTIBILITY TESTING - AUTOMATED, Reference Number 424811 - safety alert

FDA30 Sept 2026

Brand match

Medium risk

Markets

US
ELECTRONICS
Medium

VITEK 2 AST-N447 TEST KIT Product reference 424620 - safety alert

FDA4 Jun 2026

Brand match

Medium risk

Markets

US
ELECTRONICS
Medium

a product listed in the official notice - safety alert

FDA8 Oct 2025

Brand match

Medium risk

Markets

US
ELECTRONICS
Medium

a product listed in the official notice - safety alert

FDA29 Apr 2020

Brand match

Medium risk

Markets

US
ELECTRONICS
Critical

a product listed in the official notice - safety alert

FDA29 Aug 2018

Brand match

Critical risk

Markets

US
ELECTRONICS
Medium

VITEK2 GP-ID, REF 21342 IVD - safety alert

FDA15 Nov 2017

Brand match

Medium risk

Markets

US
ELECTRONICS
Medium

VIDAS Testosterone, Ref 30418 - safety alert

FDA19 Jul 2017

Brand match

Medium risk

Markets

US
ELECTRONICS
Medium

a product listed in the official notice - safety alert

FDA26 Dec 2018

Brand match

Medium risk

Markets

US
ELECTRONICS
Medium

a product listed in the official notice - safety alert

FDA26 Sept 2018

Brand match

Medium risk

Markets

US
ELECTRONICS
Critical

a product listed in the official notice - safety alert

FDA27 Dec 2017

Brand match

Critical risk

Markets

UK
ELECTRONICS
Medium

NucliSENS Lysis Buffer Extended lot for RES 76675 - safety alert

FDA15 Nov 2017

Brand match

Medium risk

Markets

US
ELECTRONICS
Medium

a product listed in the official notice - safety alert

FDA8 Mar 2023

Brand match

Medium risk

Markets

US

Weekly recall digest

Get next week's recalls before you need them.

One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.

The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.

This recall was published 27 Sept 2017. The next one won't wait for you to search.

RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.