---
title: "iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616 — FDA record Z-0024-2025 | Is It on Recall"
description: "There is an error in the Unique Device Identifier (UDI) printed on the product's distribution label."
url: https://isitonrecall.com/recall/fda-device-z-0024-2025-icast-covered-stent-6mmx16mmx120cm-model-number-42616/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616 — FDA record Z-0024-2025

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 Sep 9, 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**: iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616
- **Reason**: There is an error in the Unique Device Identifier (UDI) printed on the product's distribution label.
- **Classification**: Class II
- **Recalling firm**: Atrium Medical Corporation
- **Quantity**: 11 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0024-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0024-2025%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: 00650862426168; Lot Number: 508083; Serial Numbers: 508083031, 508083032, 508083034, 508083035, 508083036, 508083037, 508083038, 508083039, 508083040, 508083041, 508083042 |

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

## Distribution

US Nationwide distribution in the states of FL, MA, MI, OH, WA.

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

- [Alaska](https://isitonrecall.com/state/alaska/)
- [Alabama](https://isitonrecall.com/state/alabama/)
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- [North Dakota](https://isitonrecall.com/state/north-dakota/)
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- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
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- [South Dakota](https://isitonrecall.com/state/south-dakota/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Oct 16, 2024
- **Recall initiation date**: Sep 9, 2024
- **Center classification date**: Oct 7, 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-0024-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Atrium Medical Corporation records](https://isitonrecall.com/brand/atrium-medical-corporation/)