FDA Device recall Z-0502-2022
greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in tot…
- FDA Device
- Class II
- terminated
- Published 2022-01-26
On 2022-01-26 the FDA classified a Class II recall of greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in tot… by Greiner Bio One North America, citing some of the blood collection tubes show clotting due to variation of Lithium Heparin.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0502-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-12-09 |
| Published | 2022-01-26 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Greiner Bio One North America |
| Distribution | FL, IL, MO, NC, NM, NY, PA, TN, TX, VA |
Product
greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in total, REF 456087P
Reason
Some of the blood collection tubes show clotting due to variation of Lithium Heparin.
Identifiers
| code_info | Lot #B21053QG, Exp. 09/09/2022, UDI: Case: 39120017579046, Rack: 29120017579049. |
|---|
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-0502-2022%22
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