FDA Device recall Z-2485-2021
VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged
- FDA Device
- Class II
- terminated
- Published 2021-10-06
On 2021-10-06 the FDA classified a Class II recall of VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged by Greiner Bio One North America, citing blood collection tubes may experience a clotting issue.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2485-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-08-13 |
| Published | 2021-10-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Greiner Bio One North America |
| Distribution | AL, AZ, CO, CT, FL, IL, MA, MD, MI, MO, NC, NM, PA, TX, VA |
Product
VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged
Reason
Blood collection tubes may experience a clotting issue.
Identifiers
| code_info | Item Number 456279, Lot B21033DA, exp. 09/08/2022, UDI Case - 39120017571248; UDI Rack - 29120017571241 UPDATE per 9/1…Item Number 456279, Lot B21033DA, exp. 09/08/2022, UDI Case - 39120017571248; UDI Rack - 29120017571241 UPDATE per 9/10/2021 email: Item Number 456279, Lot B21053R8, exp. 11/10/2022, UDI Case -39120017571248; UDI Rack - 29120017571241. |
|---|
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-2485-2021%22
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