---
title: "DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK, 1-UP PG- Indicated for use in at... — FDA record Z-1771-2024 | Is It on Recall"
description: "Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure."
url: https://isitonrecall.com/recall/fda-device-z-1771-2024-duramax-stacked-tip-28-cm-straight-vasc-pak-1-up-pg-indicated-for-use-in-attaining-long-term-vascula/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK, 1-UP PG- Indicated for use in attaining Long-Term vascular access for He... — FDA record Z-1771-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 18, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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
- **Reason**: Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
- **Classification**: Class II
- **Recalling firm**: Angiodynamics, Inc.
- **Quantity**: 15 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1771-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1771-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: 25051684011850 Lot Numbers: 5807208 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

VA

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: May 15, 2024
- **Recall initiation date**: Mar 18, 2024
- **Center classification date**: May 3, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1771-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Angiodynamics, Inc. records](https://isitonrecall.com/brand/angiodynamics-inc/)