---
title: "17-OH Progesterone ELISA 96 well kit- An enzyme immunoassay for the quantitat... — FDA record Z-0258-2025 | Is It on Recall"
description: "The High and Low Control acceptance ranges in the Certificate of Analysis (CofA) did not match the acceptance range information on the High and Low Control Comp"
url: https://isitonrecall.com/recall/fda-device-z-0258-2025-17-oh-progesterone-elisa-96-well-kit-an-enzyme-immunoassay-for-the-quantitative-in-vitro-diagnostic/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# 17-OH Progesterone ELISA 96 well kit- An enzyme immunoassay for the quantitative in vitro diagnostic measurement of 1... — FDA record Z-0258-2025

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 Sep 13, 2024. 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**: 17-OH Progesterone ELISA 96 well kit- An enzyme immunoassay for the quantitative in vitro diagnostic measurement of 17-OH Progesterone (17-OHP) in serum or plasma Model/Catalog Number: EIA-1292
- **Reason**: The High and Low Control acceptance ranges in the Certificate of Analysis (CofA) did not match the acceptance range information on the High and Low Control Component labels. Due to the defect, the device failed to provide results, which may result in a delay in obtaining test results and a remote chance of an adverse health risk.
- **Classification**: Class III
- **Recalling firm**: DRG International, Inc.
- **Quantity**: 504 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0258-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0258-2025%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 Code: 04048474012927 (DRG Instruments GmbH) lots: 22K024 and 22K034 |

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

## Distribution

AZ, CA, NH Foreign: Austria Belgium Georgia Germany Greece India Irak Italy Netherlands Poland Romania Russia Singapore Spain Tunesia Vietnam

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

- [Arizona](https://isitonrecall.com/state/arizona/)
- [California](https://isitonrecall.com/state/california/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [New Hampshire](https://isitonrecall.com/state/new-hampshire/)

## Dates in the source

- **Report date**: Nov 6, 2024
- **Recall initiation date**: Sep 13, 2024
- **Center classification date**: Oct 29, 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-0258-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [DRG International, Inc. records](https://isitonrecall.com/brand/drg-international-inc/)