Greiner Bio-One North America, Inc.: Medical Device Recall in 2024 - (Recall #: Z-2375-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.
Product Description:

VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged

Product Classification:

Class II

Date Initiated: May 14, 2024
Date Posted: July 24, 2024
Recall Number: Z-2375-2024
Event ID: 94817
Reason for Recall:

The firm received reports that some blood collection tubes have experienced issues with clotting and poor separation due to missing additive. The failure of the device would likely require sample recollection which could result in a delay of treatment.

Status: Ongoing
Product Quantity: 1,008,000pcs (840 cartons)
Code Information:

Item Number: 455071P; UDI Case label: 39120017573068; UDI Rack label: 29120017573061; Lot Number: B24013MV

Distribution Pattern:

Nationwide Distribution to states of: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WV and WY.

Voluntary or Mandated:

Voluntary: Firm initiated