fda_recall · device_recall · high
Accriva Diagnostics, Inc. — Class II recall: directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: D…
- Event date
- 2026-06-24 00:00:00Z
- Observed
- 2026-07-09 22:52:09Z
- Source ID
- Z-2460-2026
- Payload hash
- c750be044c0d381dabd7f07d…
Summary
Assayed Whole blood control contains labeling with incorrect performance range. Status: Ongoing.
Entities
Informational only. Not legal, financial, or medical advice.