---
title: "C-Peptide ELISA : IVD measurement of C-Peptide in serum, plasma (EDTA-, hepar... — FDA record Z-0896-2022 | Is It on Recall"
description: "ODs of the standards too low(< 0.6 ODmax) may cause invalid runs, delayed patient results are possible"
url: https://isitonrecall.com/recall/fda-device-z-0896-2022-c-peptide-elisa-ivd-measurement-of-c-peptide-in-serum-plasma-edta-heparin-or-citrate-plasma-and-urin/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# C-Peptide ELISA : IVD measurement of C-Peptide in serum, plasma (EDTA-, heparin- or citrate plasma) and urine. Catalo... — FDA record Z-0896-2022

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 Dec 21, 2021. 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**: C-Peptide ELISA : IVD measurement of C-Peptide in serum, plasma (EDTA-, heparin- or citrate plasma) and urine. Catalog # EIA-1293
- **Reason**: ODs of the standards too low(< 0.6 ODmax) may cause invalid runs, delayed patient results are possible
- **Classification**: Class II
- **Recalling firm**: DRG International, Inc.
- **Quantity**: 3 Kits
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0896-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0896-2022%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# / Expiration dates: 20K061 / 2022-06-30 20K071 / 2022-07-31 20K081 / 2022-08-31 |

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

## Distribution

NY

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

- [New York](https://isitonrecall.com/state/new-york/)

## Dates in the source

- **Report date**: Apr 13, 2022
- **Recall initiation date**: Dec 21, 2021
- **Center classification date**: Apr 7, 2022
- **Termination date**: Feb 12, 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-0896-2022%22)

## Related records

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