United StatesGreiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2% blood collection tubes (REF 454322, Lot B250139Q, Expiration 01/09/2026; UDI-DI: 29120017574488 (Rack), 39120017574485 (Case)) are affected. The tubes were manufactured with the label applied too high, shifting the printed fill level mark upward, which could cause unnecessary sample rejection and repeat collections.
What's being recalled
Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2%, REF: 454322
Recalling firm: Greiner Bio-One North America, Inc., Monroe, NC, United States.
How to identify it
UDI-DI: 29120017574488(Rack), 39120017574485(Case). Lot: B250139Q, Expiration: 01/09/2026
The hazard
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.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)