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FDA
Food and Drug Administration · Recall Z-2894-2026 · Jul 1, 2026

5-PLASMA Bivalirudin AMR Verification Kit, Model Number 5D-45905

Aniara Diagnostica LLC

The hazard

Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin in the controls, calibrators, and linearity values. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

5-PLASMA Bivalirudin AMR Verification Kit, Model Number 5D-45905

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model UDI-DI: 05070002420378Model Lot Number: KE132603UPC 05070002420378

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.