VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red… — Class II medical device recall Z-2375-2024
Ongoing recall by Greiner Bio-One North America, Inc., reported 2024-07-24, distributed nationwide. The firm received reports that some blood collection tubes have experienced issues with clotting and poor sepa
| Recall number | Z-2375-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Greiner Bio-One North America, Inc., Monroe, NC, United States |
| Recall initiated | 2024-05-14 |
| Classified | 2024-07-17 |
| Reported by FDA | 2024-07-24 |
| Distributed | Nationwide (US) |
| UPC / GTIN / UDI-DI | 29120017573061, 39120017573068 |
| Lot numbers | B24013MV |
| Model numbers | 455071P |
Product
VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged
Reason for recall
The firm received reports that some blood collection tubes have experienced issues with clotting and poor separation due to missing additive. The failure of the device would likely require sample recollection which could result in a delay of treatment.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2375-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.