directCHECK ACT-LR whole blood quality control: recall status

Notice names this product. Accriva Diagnostics’s directCHECK ACT-LR whole blood quality control is named in FDA Class II recall Z-2460-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Assayed Whole blood control contains labeling with incorrect performance range. Identifying details: Lot #: A6DLA001 Unique Device Identifier: 10711234170373. Units affected: 6,060. Status: Ongoing.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: directCHECK ACT-LR whole blood quality control
Company / brand: Accriva Diagnostics
Lot / serial / date codes: Lot #: A6DLA001 Unique Device Identifier: 10711234170373
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.

Agency product description and boundaries

directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

Brand: Accriva Diagnostics

Recalls naming this model

FDA Class II · Medical device · June 24, 2026

directCHECK ACT-LR whole blood quality control recall — Accriva Diagnostics, Inc.

Assayed Whole blood control contains labeling with incorrect performance range.

Company / brand: Accriva Diagnostics recalls

Affected product: directCHECK ACT-LR whole blood quality control recall status

Official ID Z-2460-2026 · Official record ↗

See all Accriva Diagnostics recalls →

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.