VACUETTE SAFELINK (Greiner Bio-One) – Blood Leakage Risk (2024)
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
VACUETTE SAFELINK, REF: 450210
Brand
Greiner Bio-One GmbH Bad Haller Strase
Lot Codes / Batch Numbers
UDI-DI: 19120049207487, Lot: A240338Q, Expiration Date: 270215
Products Sold
UDI-DI: 19120049207487, Lot: A240338Q, Expiration Date: 270215
Greiner Bio-One GmbH Bad Haller Strase is recalling VACUETTE SAFELINK, REF: 450210 due to 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 devi. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
On 11/19/2024, customers and distributors were mailed and emailed recall notices asking them to do the following: 1) Stop using and isolate affected devices. 2) If the product has been further distributed or transferred to another location, notify those locations of the recall, and advise the name/location in the provided space on the attached Product Disposition Site Confirmation. 3) Complete and return the Product Disposition Site Confirmation form via email to recalls.us@gbo.com If you have additional questions, contact the firm's Technical Service Department at 800-515-8112.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026