FDA Device recall Z-2507-2021
Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged
- FDA Device
- Class II
- terminated
- Published 2021-09-29
On 2021-09-29 the FDA classified a Class II recall of Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged by Greiner Bio One North America, citing complaint of tubes clotting due to variation of anticoagulant and/or tubes have low vacuum.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2507-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-08-20 |
| Published | 2021-09-29 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Greiner Bio One North America |
| Distribution | US |
Product
Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged
Reason
Complaint of tubes clotting due to variation of anticoagulant and/or tubes have low vacuum.
Identifiers
| code_info | Lot # B210533B Expiration 05/10/22 and B210439J Expiration 04/13/2022. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2507-2021%22
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