---
title: "BioPlex 2200 REF 12000670 ToRC IgM Reagent Pack — FDA record Z-1096-2022 | Is It on Recall"
description: "Performance concerns for the CMV IgM analyte. Analyte has demonstrated variable elevated background depending on the handling of the reagent pack."
url: https://isitonrecall.com/recall/fda-device-z-1096-2022-bioplex-2200-ref-12000670-torc-igm-reagent-pack/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# BioPlex 2200 REF 12000670 ToRC IgM Reagent Pack — FDA record Z-1096-2022

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 Apr 14, 2022. 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**: BioPlex 2200 REF 12000670 ToRC IgM Reagent Pack
- **Reason**: Performance concerns for the CMV IgM analyte. Analyte has demonstrated variable elevated background depending on the handling of the reagent pack.
- **Classification**: Class II
- **Recalling firm**: Bio-Rad Laboratories, Inc.
- **Quantity**: 348 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1096-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1096-2022%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 | Model/Catalog Number: 12000670 UDI-DI (GTIN) Code: 03610520992715 Lot Number: 301388 |

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

## Distribution

Worldwide distribution - U.S. Nationwide distribution in the states of AR, AZ, CA, FL, HI, IA, IL, MI, MN, NE, NY, TN, TX, and WA. The countries of Czech Republic, France, Germany, and Italy.

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

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: May 25, 2022
- **Recall initiation date**: Apr 14, 2022
- **Center classification date**: May 16, 2022

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-1096-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Bio-Rad Laboratories, Inc. records](https://isitonrecall.com/brand/bio-rad-laboratories-inc/)
