---
title: "DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0c... — FDA record Z-0668-2022 | Is It on Recall"
description: "Outer packaging (outer pouch) is not sealed compromising sterility and result in potential risk of patient infection, which could lead to revision surgery"
url: https://isitonrecall.com/recall/fda-device-z-0668-2022-duramatrix-onlay-collagen-dura-substitute-membrane-4-inches-x-5-inches-10-0cm-x-12-5cm-ref-cdslm45/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0cm x 12.5cm) REF: CDSLM45 — FDA record Z-0668-2022

Reported terminated

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 Dec 13, 2021. 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**: DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0cm x 12.5cm) REF: CDSLM45
- **Reason**: Outer packaging (outer pouch) is not sealed compromising sterility and result in potential risk of patient infection, which could lead to revision surgery
- **Classification**: Class II
- **Recalling firm**: Collagen Matrix, Inc.
- **Quantity**: 68 units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0668-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0668-2022%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 | Model Number CDSLM45 Lot Number 2107292022 Exp Date:7/31/2024 UDI: (01)00813954020273(17)240731(10)2107292022 |

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

## Distribution

DuraMatrix-Onlay distributed US Nationwide in the states of FL, IN, Puerto Rico, and the countries of Canada, Chile, and Colombia. RESODURA matrix onlay distributed in Germany.

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/)
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## Dates in the source

- **Report date**: Mar 2, 2022
- **Recall initiation date**: Dec 13, 2021
- **Center classification date**: Feb 24, 2022
- **Termination date**: Sep 18, 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-0668-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Collagen Matrix, Inc. records](https://isitonrecall.com/brand/collagen-matrix-inc/)
