Class II

Medical Device Recall: VACUETTE SAFELINK, REF: 450210

Greiner Bio-One GmbH · November 19, 2024

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.

Distribution

US Nationwide distribution in the states of IL, PA.

States Affected

NATIONWIDE

Quantity Affected

188,800 pcs

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0802-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Greiner Bio-One GmbH Medical Device Recall: VACUETTE SAFELINK, REF: 450210 | SafeCheck