FDA recall Z-2362-2026

The Binding Site Group, Ltd. · Class II · device

Product

Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids used in conjunction with the EXENT assays.

Reason for recall

It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being measured. The potential clinical hazards include false or missed detection of M-protein (false positive); and falsely elevated or decreased M-protein concentration.

Distribution

US Nationwide distribution.

Key facts

Status
Ongoing
Initiation date
2026-04-16
Report date
2026-06-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Birmingham, N/A, United Kingdom

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2362-2026