Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate Recalled by Greiner Bio-One North America, Inc. Due to Complaint of tubes clotting due to variation of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Greiner Bio-One North America, Inc. directly.
Affected Products
Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged
Quantity: 956,400
Why Was This Recalled?
Complaint of tubes clotting due to variation of anticoagulant and/or tubes have low vacuum.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Greiner Bio-One North America, Inc.
Greiner Bio-One North America, Inc. has 16 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report