HomeMedical Device recalls
Medium severity

Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2%, REF: 454322

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateAugust 08, 2025
ReportedNovember 05, 2025
Recalling firmGreiner Bio-One North America, Inc.
Country / regionUnited States NC

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.

Affected products

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