---
title: "The Binding Site Group, Ltd. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search The Binding Site Group, Ltd. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/the-binding-site-group-ltd/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# The Binding Site Group, Ltd. recall records

**1** reported ongoing

2 records in this archive. Latest source date Apr 16, 2026.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## Records and reported status

Apr 16, 2026 FDA device enforcement

### [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 i...](https://isitonrecall.com/recall/fda-device-z-2362-2026-brand-name-exent-analyser-product-name-exent-analyser-model-catalog-number-ie800-a-software-version/)

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); ...

Class II Reported ongoing

Distribution: US Nationwide distribution.

[Official source for Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Ve...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2362-2026%22)

Oct 15, 2021 FDA device enforcement

### [Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the SPAPLUS) (x10) REF LK018.10S](https://isitonrecall.com/recall/fda-device-z-0274-2022-freelite-human-lambda-free-kit-for-use-on-the-spaplus-ref-lk018-s-freelite-human-lambda-free-kit-for/)

Due to calibration curves producing a higher activity than routinely expected and that there may be a decrease in separation between calibrator point 5 and calibrator point 6, which can be exacerbated with calibrator 6 activity reaches the optical ceiling o...

Class II Reported terminated

Distribution: U.S.: CA, CO, FL, IL, IN, KY, LA, MI, NY, OK, SD, TX and VA. O.U.S.: Canada

[Official source for Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Ki...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0274-2022%22)

## Reasons in these listed records

- 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...
- Due to calibration curves producing a higher activity than routinely expected and that there may be a decrease in separation between calibrator point 5 and calibrator point 6, which can be exacerbated with calibrator 6 activity reaches the optical ceiling of the SPA+ analyzer.

These examples come from this result page and are not a ranking of every recall reason.

## Checking The Binding Site Group, Ltd.

### Is there a recall on the binding site group, ltd. right now?

This archive contains 2 records, including 1 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search The Binding Site Group, Ltd.](https://isitonrecall.com/check/?q=The%20Binding%20Site%20Group%2C%20Ltd.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
