Kremsmunster, Austria
Greiner Bio-One GmbH recalls
1 recall recorded since 2018, most recently on 19 November 2024. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 19 November 2024
- Reason
- 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.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0802-2025
- VACUETTE SAFELINK, REF: 450210
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.