Greiner Bio-One North America, Inc. Greiner Bio-One VACUETTE TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Greiner Bio-One VACUETTE TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged
Brand
Greiner Bio-One North America, Inc.
Lot Codes / Batch Numbers
Lot # B210533B Expiration 05/10/22 and B210439J Expiration 04/13/2022.
Products Sold
Lot # B210533B Expiration 05/10/22 and B210439J Expiration 04/13/2022.
Greiner Bio-One North America, Inc. is recalling Greiner Bio-One VACUETTE TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sa due to Complaint of tubes clotting due to variation of anticoagulant and/or tubes have low vacuum.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Complaint of tubes clotting due to variation of anticoagulant and/or tubes have low vacuum.
Recommended Action
Per FDA guidance
A letter was sent on August 20, 2021 with the following actions: Necessary actions: We need your assistance to address this recall. Please perform the following steps. " Stop using the above-mentioned product (concerned item/lot) immediately and isolate defective products in your facility. " Assess risks and consequences for the use of this defective product in accordance with your procedures and take appropriate action. " Complete the attached Product Disposition Site Confirmation form and fax to Greiner Bio-One North America, Inc. at 800.726.0052 or email to patech@gbo.com. This form is to confirm that you have discarded/destroyed all products from these items/lots. We will replace the product after the completed form is sent to Greiner. If you have additional questions, please call our Technical Service at 800-515-8112.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026