greiner bio-one VACUETTE TUBE — Class II medical device recall Z-0502-2022
Terminated recall by Greiner Bio-One North America, Inc., reported 2022-01-26, distributed in FL, IL, MO, NC, NM, NY, PA, TN…. Some of the blood collection tubes show clotting due to variation of Lithium Heparin.
| Recall number | Z-0502-2022 |
|---|---|
| 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 | 2021-12-09 |
| Classified | 2022-01-18 |
| Reported by FDA | 2022-01-26 |
| Terminated | 2023-10-10 |
| Distributed | FL, IL, MO, NC, NM, NY, PA, TN, TX, VA |
| Quantity | 889,200 units |
| UPC / GTIN / UDI-DI | 29120017579049, 39120017579046 |
| Lot numbers | B21053QG |
| Model numbers | 456087P |
| Expiration dates | 2022-09-09 |
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 for recall
Some of the blood collection tubes show clotting due to variation of Lithium Heparin.
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-0502-2022. 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.