FDA Device recall Z-1714-2020
VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322
- FDA Device
- Class II
- terminated
- Published 2020-04-22
On 2020-04-22 the FDA classified a Class II recall of VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322 by Greiner Bio One North America, citing concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have inconsistent amounts of the 2.3% sodium citrate.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1714-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-03-12 |
| Published | 2020-04-22 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Greiner Bio One North America |
| Distribution | US |
Product
VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.
Reason
Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have inconsistent amounts of the 2.3% sodium citrate.
Identifiers
| code_info | Item no. 454322. Lot no. B1908355. DI no. (01)29120017574488 (17) 200809 (10)B1908355. |
|---|
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-1714-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.