---
title: "BD Kiestra\" Isolate Suspension Cuvette Array; Catalog No.: 246100; — FDA record Z-0484-2026 | Is It on Recall"
description: "The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instr"
url: https://isitonrecall.com/recall/fda-device-z-0484-2026-bd-kiestra-isolate-suspension-cuvette-array-catalog-no-246100/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100; — FDA record Z-0484-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Oct 23, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

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/).

## What the record says

- **Product**: BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
- **Reason**: The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an error state and the cuvettes cannot be used.
- **Classification**: Class II
- **Recalling firm**: Becton Dickinson & Co.
- **Quantity**: 29,760 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0484-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0484-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Catalog No.: 246100; UDI-DI: 30382902461006; Lot Number: LM245590, LM245592, LM245593, LM245594, LM245666; |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide - US Nationwide distribution in the states of CO, CT, KY, NJ, TN, TX, UT and the countries of Belgium, Singapore, Taiwan, Germany, Switzerland.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Nov 19, 2025
- **Recall initiation date**: Oct 23, 2025
- **Center classification date**: Nov 7, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0484-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Becton Dickinson & Co. records](https://isitonrecall.com/brand/becton-dickinson-co/)