[Recalled] DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK, 1-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028191 — Tri-Ball Tunneler may contain loosely affixed me
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK, 1-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028191 |
|---|---|
| Brand / manufacturer | Angiodynamics, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1771-2024 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 18 March 2024 |
| EAN / barcode | 25051684011850 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Angiodynamics, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.