---
title: "V8 Immunodisplacement Kit REF 1803 — FDA record Z-1244-2022 | Is It on Recall"
description: "Due to microbial growth causing interference with interpretation."
url: https://isitonrecall.com/recall/fda-device-z-1244-2022-v8-immunodisplacement-kit-ref-1803/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# V8 Immunodisplacement Kit REF 1803 — FDA record Z-1244-2022

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 6, 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**: V8 Immunodisplacement Kit REF 1803
- **Reason**: Due to microbial growth causing interference with interpretation.
- **Classification**: Class II
- **Recalling firm**: Helena Laboratories, Corp.
- **Quantity**: 51 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1244-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1244-2022%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 Number: 1803 UDI Codes: +M52518030/SS73-21-1803/14D20230831Z +M52518030/SS71-21-1803/14D20230830X Lot 3-21-1803 Lot 1-22-1803 |

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

## Distribution

U.S.: FL, MO, OH, and TX O.U.S.: Canada, Uruguay, and Vietnam,

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

- [Florida](https://isitonrecall.com/state/florida/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Jun 15, 2022
- **Recall initiation date**: Apr 6, 2022
- **Center classification date**: Jun 7, 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-1244-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Helena Laboratories, Corp. records](https://isitonrecall.com/brand/helena-laboratories-corp/)