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[Recalled] VIDAS LH, REF 30406-01 — bioMerieux has been receiving an increasing number of complaints linked to a VI… | FDA 2021-09-22

recall fda device united-states

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

ProductVIDAS LH, REF 30406-01
Brand / manufacturerbioMerieux, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0433-2022
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date22 September 2021
EAN / barcode03573026156930

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: bioMerieux has been receiving an increasing number of complaints linked to a VIDAS substrate error. It prevents the test from being run, therefore leads to potential delayed results as the user must run another test.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from bioMerieux, Inc.

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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