PlainRecalls
FDA Devices Moderate Class II Ongoing

VIDAS Clostridium Difficile GDH, REF 30125-01

Reported: January 5, 2022 Initiated: September 22, 2021 #Z-0426-2022

Product Description

VIDAS Clostridium Difficile GDH, REF 30125-01

Reason for Recall

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.

Details

Recalling Firm
bioMerieux, Inc.
Units Affected
50
Distribution
US Nationwide distribution.
Location
Durham, NC

Frequently Asked Questions

What product was recalled?
VIDAS Clostridium Difficile GDH, REF 30125-01. Recalled by bioMerieux, Inc.. Units affected: 50.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 5, 2022. Severity: Moderate. Recall number: Z-0426-2022.