---
title: "directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number:... — FDA record Z-2460-2026 | Is It on Recall"
description: "Assayed Whole blood control contains labeling with incorrect performance range."
url: https://isitonrecall.com/recall/fda-device-z-2460-2026-directcheck-act-lr-whole-blood-quality-control-level-2-model-catalog-number-dcglr-2/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2 — FDA record Z-2460-2026

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 30, 2026. 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**: directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
- **Reason**: Assayed Whole blood control contains labeling with incorrect performance range.
- **Classification**: Class II
- **Recalling firm**: Accriva Diagnostics, Inc.
- **Quantity**: 6060
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2460-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2460-2026%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 #: A6DLA001 Unique Device Identifier: 10711234170373 |

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

## Distribution

Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, FL, GA, ID, IL, IN, KY, MA, MD, MI, MN, MO, MT, NC, NJ, NM, NY, OH, OK, PA, SC, TN, TX, VA, VT, WA, WI, WV and the countries of Canada, Hong Kong, Spain.

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

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Nevada](https://isitonrecall.com/state/nevada/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jun 24, 2026
- **Recall initiation date**: Apr 30, 2026
- **Center classification date**: Jun 16, 2026

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-2460-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Accriva Diagnostics, Inc. records](https://isitonrecall.com/brand/accriva-diagnostics-inc/)
