Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0802-2025 — VACUETTE SAFELINK, REF: 450210

U.S. FDA — Device Enforcement · Austria · 2024-11-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0802-2025
Date of alert
2024-11-19
Country / jurisdiction
Austria
Risk level
Class II
Risk type
recall
Brand
Greiner Bio-One GmbH
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
19120049207487
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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