Kremsmunster, N/A, Austria
C.A. Greiner & Sohne Gesellschaftmbh recalls
2 recalls recorded since 2018, most recently on 27 July 2020. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)1
Terminated or completed1
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 27 July 2020
- Reason
- Sample leaking from the sleeve covering the needle inside the cannula
- Distribution
- US Nationwide distribution including in the states of UT, TN.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2911-2020
- Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is intended for use in routine specimen withdrawal from specimen collection bags or bottles through needleless cannula ports.
Terminated Class II Medical devices
- Recall started
- 3 April 2020
- Terminated
- 25 July 2021
- Reason
- While transferring blood the needle may dislodged and remain in the tube stopper which may cause needle stick injury or blood leakage.
- Distribution
- *requested 4/15/2020
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2116-2020
- VACUETTE Blood Transfer Unit. Lot no. A19024NX. Expiration date: 2022-02-07 - Product Usage: The Blood Transfer Unit is used to transfer blood from a syringe into the evacuated blood collection tube.
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.