Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3 — Class II medical device recall Z-2507-2021
Terminated recall by Greiner Bio-One North America, Inc., reported 2021-09-29, distributed nationwide. Complaint of tubes clotting due to variation of anticoagulant and/or tubes have low vacuum.
| Recall number | Z-2507-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Greiner Bio-One North America, Inc., Monroe, NC, United States |
| Recall initiated | 2021-08-20 |
| Classified | 2021-09-22 |
| Reported by FDA | 2021-09-29 |
| Terminated | 2023-10-04 |
| Distributed | Nationwide (US) |
| Quantity | 956,400 |
| Lot numbers | B210439J, B210533B |
| Expiration dates | 2022-04-13, 2022-05-10 |
Product
Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged
Reason for recall
Complaint of tubes clotting due to variation of anticoagulant and/or tubes have low vacuum.
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-2507-2021. 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.