device · product 1 of 1
directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
- Recall number
- Z-2460-2026
- Initiated
- April 30, 2026
- Classification
- Class II
- Status
- Ongoing
- Recalling firm
- Accriva Diagnostics, Inc.
- Quantity
- 6060
App-derived interpretation
labeling with incorrect
Official device-enrichment evidence · Sourced
Process control
Inspect official wording and provenance
Reason for recall
Assayed Whole blood control contains labeling with incorrect performance range.
Code information
Lot #: A6DLA001 Unique Device Identifier: 10711234170373
Distribution pattern
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.