Aniara Diagnostica LLC: 5-PLASMA Bivalirudin Control, Model Number 5D-44905
Read the official notice at FDA (device) →
Get alerts for Aniara Diagnostica
The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.
- Company / brand
- Aniara Diagnostica LLC
- Product
- 5-PLASMA Bivalirudin Control, Model Number 5D-44905
- Reason / 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.
- Classification
- Class II
- Status
- Ongoing
- Distribution / sold at
- US Nationwide distribution in the states of IL, NC, TN.
- Recall initiated
- 2026-07-01
- Code info
- UDI-DI: 05070002420385, Lot Number: KE132602
- Product quantity
- 9 units
- Voluntary mandated
- Voluntary: Firm initiated
- City
- West Chester
- State
- OH
- Country
- United States
- Event id
- 99344
Free daily digest + "My products" watchlist