Greiner Bio-One North America, Inc. recalls Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2%
- Recalling company
- Greiner Bio-One North America, Inc.
- Product
- Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2%, REF: 454322
- Reason
- Blood collection tubes were manufactured with the label applied too high on the tube, which shifted the printed fill level mark upward, which could result in unnecessary sample rejection and repeat collections.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Aug 8, 2025
- Reported
- Nov 5, 2025
- Distribution
- US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 504,000
- Lot / codes
- UDI-DI: 29120017574488(Rack), 39120017574485(Case). Lot: B250139Q, Expiration: 01/09/2026
- Company location
- Monroe, NC
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0408-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0408-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.