Greiner Bio-One North America, Inc.: Medical Device Recall in 2012 - (Recall #: Z-2154-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

3mL 9NC Coagulation Sodium Citrate 3.2%, Item #454334, Greiner Bio-One North America Inc., 4238 Capital Drive, Monroe, NC 28110. Intended Use: Venous blood collection tubes.

Product Classification:

Class II

Date Initiated: July 2, 2012

Date Posted: August 15, 2012

Recall Number: Z-2154-2012

Event ID: 62595

Reason for Recall:

Part of the lot received a lower concentration of citrate solution which may cause falsely lower values for common coagulation tests.

Status: Terminated

Product Quantity: 838.9 cases (1,006,700 pieces)

Code Information:

Lot #B041206

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated