Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75 Recalled by Greiner Bio-One North America, Inc. Due to VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate...
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
VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged - Product Usage: indicated for use in collection and transport of venous whole blood for coagulation testing.
Quantity: 1,049,700 units
Why Was This Recalled?
VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% may show insufficient draw volume of the tubes, which could produce erroneous results for prothrombin time, activated partial thromboplastin time, and fibrinogen assays.
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.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report