greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA — Class II medical device recall Z-1583-2023
Completed recall by Greiner Bio-One North America, Inc., reported 2023-05-24, distributed nationwide. Some of the tubes may be incorrectly labeled.
| Recall number | Z-1583-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Greiner Bio-One North America, Inc., Monroe, NC, United States |
| Recall initiated | 2023-03-31 |
| Classified | 2023-05-12 |
| Reported by FDA | 2023-05-24 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 29120017576499, 39120017576496 |
| Lot numbers | B220533J |
| Model numbers | 456003 |
| Expiration dates | 2023-10-31 |
Product
greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA, 13x100 pink cap-black ring, non-ridged, 24 racks of 50 pcs., 1200 pcs in total, Item #456003
Reason for recall
Some of the tubes may be incorrectly labeled.
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-1583-2023. 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.