Greiner VACUETTE North America Serum Blood Collection Tubes Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Serum Blood Collection Tubes
Brand
Greiner VACUETTE North America
Lot Codes / Batch Numbers
Item #455071, Lot #B040513 and Item #455092, Lot #B040503
Products Sold
Item #455071, Lot #B040513 and Item #455092, Lot #B040503
Greiner VACUETTE North America is recalling Serum Blood Collection Tubes due to Serum Blood Collection tubes found with excess of Blood Clot Accelerator (BCA) solution.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Serum Blood Collection tubes found with excess of Blood Clot Accelerator (BCA) solution.
Recommended Action
Per FDA guidance
Consignees were notified by letter on 07/28/2005.
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