---
title: "Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Cata... — FDA record Z-1896-2026 | Is It on Recall"
description: "Potential for product to contain foreign matter, confirmed to be inspect fragments."
url: https://isitonrecall.com/recall/fda-device-z-1896-2026-avitene-ultrafoam-microfibrillar-collagen-hemostat-8cm-x-6-25cm-x-1cm-catalog-number-1050030/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030. — FDA record Z-1896-2026

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 25, 2026. 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**: Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.
- **Reason**: Potential for product to contain foreign matter, confirmed to be inspect fragments.
- **Classification**: Class II
- **Recalling firm**: Davol, Inc.
- **Quantity**: 1,622 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1896-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1896-2026%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 | Catalog Number: 1050030. UDI: (01)00801741010538(17)270728(10)WBJS0055. Lot Number: WBJS0055. Expiration Date: 07/28/2027 |

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

## Distribution

Worldwide distribution - US Nationwide and the countries of China, South Korea.

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

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## Dates in the source

- **Report date**: Apr 29, 2026
- **Recall initiation date**: Mar 25, 2026
- **Center classification date**: Apr 21, 2026

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-1896-2026%22)

## Related records

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