DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK — Class II medical device recall Z-1772-2024
Ongoing recall by Angiodynamics, Inc., reported 2024-05-15, distributed in VA. XXX
| Recall number | Z-1772-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Angiodynamics, Inc., Queensbury, NY, United States |
| Recall initiated | 2024-03-18 |
| Classified | 2024-05-03 |
| Reported by FDA | 2024-05-15 |
| Distributed | VA |
| Quantity | 285 units |
| UPC / GTIN / UDI-DI | 25051684011935 |
| Lot numbers | 5807195, 5807196 |
Product
DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK, 5-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028195
Reason for recall
XXX
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-1772-2024. 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.