FDA Device recall Z-3027-2020
VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator, Item Number: 456018P - Product Usage: are used to collect, transport, and process bl…
- FDA Device
- Class II
- terminated
- Published 2020-10-07
On 2020-10-07 the FDA classified a Class II recall of VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator, Item Number: 456018P - Product Usage: are used to collect, transport, and process bl… by Greiner Bio One North America, citing blood collection tubes experienced an issue with separation and clotting.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3027-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-08-28 |
| Published | 2020-10-07 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Greiner Bio One North America |
| Distribution | US |
Product
VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator, Item Number: 456018P - Product Usage: are used to collect, transport, and process blood for testing serum, plasma or whole blood in the clinical laboratory.
Reason
Blood collection tubes experienced an issue with separation and clotting
Identifiers
| code_info | Lot Number: B2003399 |
|---|
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-3027-2020%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.