---
title: "meridian bioscience immunocard STAT! Rotavirus test, REF 750030, 30 tests/kit... — FDA record Z-0678-2022 | Is It on Recall"
description: "The product was incorrectly shipped at room temperature rather than refrigerated."
url: https://isitonrecall.com/recall/fda-device-z-0678-2022-meridian-bioscience-immunocard-stat-rotavirus-test-ref-750030-30-tests-kit-box-the-immunocard-stat-r/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# meridian bioscience immunocard STAT! Rotavirus test, REF 750030, 30 tests/kit box. The ImmunoCard STAT! Rotavirus Imm... — FDA record Z-0678-2022

Reported terminated

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 Jan 25, 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**: meridian bioscience immunocard STAT! Rotavirus test, REF 750030, 30 tests/kit box. The ImmunoCard STAT! Rotavirus Immunoassay is a rapid in vitro qualitative procedure for the detection of rotavirus antigen in human stool. The test can be used to aid in the diagnosis of rotavirus associated gastroenteritis.
- **Reason**: The product was incorrectly shipped at room temperature rather than refrigerated.
- **Classification**: Class II
- **Recalling firm**: MEDLINE INDUSTRIES, LP - Northfield
- **Quantity**: 19 kits
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0678-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0678-2022%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 | Lot numbers 750030M481, Exp. 4/29/2022; 750030N482, Exp. 12/2/2022; and 750030N483, Exp. 5/17/2023. |

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

## Distribution

US Distribution was made to IL, FL, LA, MS, NC, OH, and TX.

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/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Louisiana](https://isitonrecall.com/state/louisiana/)
- [Mississippi](https://isitonrecall.com/state/mississippi/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Mar 2, 2022
- **Recall initiation date**: Jan 25, 2022
- **Center classification date**: Feb 24, 2022
- **Termination date**: Jan 9, 2023

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-0678-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MEDLINE INDUSTRIES, LP - Northfield records](https://isitonrecall.com/brand/medline-industries-lp-northfield/)