FDA Device recall Z-2116-2020
VACUETTE Blood Transfer Unit
- FDA Device
- Class II
- terminated
- Published 2020-06-03
On 2020-06-03 the FDA classified a Class II recall of VACUETTE Blood Transfer Unit by C A Greiner And Sohne Gesellschaftmbh, citing while transferring blood the needle may dislodged and remain in the tube stopper which may cause needle stick injury or blood leakage.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2116-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-04-03 |
| Published | 2020-06-03 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | C A Greiner And Sohne Gesellschaftmbh |
| Distribution | n/a |
Product
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.
Reason
While transferring blood the needle may dislodged and remain in the tube stopper which may cause needle stick injury or blood leakage.
Identifiers
| code_info | Item no. 450225. UDI no. 39120017577547 and 29120017577540. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2116-2020%22
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