Greiner Bio-One GmbH: Medical Device Recall in 2025 - (Recall #: Z-0802-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

VACUETTE SAFELINK, REF: 450210

Product Classification:

Class II

Date Initiated: November 19, 2024

Date Posted: January 15, 2025

Recall Number: Z-0802-2025

Event ID: 95748

Reason for Recall:

The VACUETTE SAFELINK Holder with male luer lock may leak blood due to the protective rubber sleeve bunching up and not retracting when using the device.

Status: Ongoing

Product Quantity: 188,800 pcs

Code Information:

UDI-DI: 19120049207487, Lot: A240338Q, Expiration Date: 270215

Distribution Pattern:

US Nationwide distribution in the states of IL, PA.

Voluntary or Mandated:

Voluntary: Firm initiated