---
title: "Detector H. Pylori, Catalog Number IHP-30 — FDA record Z-0702-2024 | Is It on Recall"
description: "Labeling for affected lots incorrectly indicates the expiration date is 10/31/2023. However, the correct expiration date is 10/31/2022. Use of the product after"
url: https://isitonrecall.com/recall/fda-device-z-0702-2024-detector-h-pylori-catalog-number-ihp-30/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Detector H. Pylori, Catalog Number IHP-30 — FDA record Z-0702-2024

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 Aug 25, 2023. 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**: Detector H. Pylori, Catalog Number IHP-30
- **Reason**: Labeling for affected lots incorrectly indicates the expiration date is 10/31/2023. However, the correct expiration date is 10/31/2022. Use of the product after its expiration may cause false positive, false negative, or invalid results.
- **Classification**: Class II
- **Recalling firm**: Immunostics, Inc.
- **Quantity**: 10 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0702-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0702-2024%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 | UDI-DI 10722355002023 Lots 0821132-2 0821132-3 0821132-4 Incorrect label Expiration: 2023-10-31 Correct Expiration: 2022-10-31 |

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

## Distribution

Product distributed to CA and MO.

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

- [California](https://isitonrecall.com/state/california/)
- [Missouri](https://isitonrecall.com/state/missouri/)

## Dates in the source

- **Report date**: Jan 17, 2024
- **Recall initiation date**: Aug 25, 2023
- **Center classification date**: Jan 10, 2024

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-0702-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Immunostics, Inc. records](https://isitonrecall.com/brand/immunostics-inc/)