---
title: "GS0008 2Y - Burn Pack - STL, Item Number 880082025 — FDA record Z-0070-2024 | Is It on Recall"
description: "Medical convenience kit contains Zimmer Dermatome Blades which were recalled by Zimmer due to 38 complaints received related to skin grafts being thin and non-u"
url: https://isitonrecall.com/recall/fda-device-z-0070-2024-gs0008-2y-burn-pack-stl-item-number-880082025/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# GS0008 2Y - Burn Pack - STL, Item Number 880082025 — FDA record Z-0070-2024

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 Sep 11, 2023. 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**: GS0008 2Y - Burn Pack - STL, Item Number 880082025
- **Reason**: Medical convenience kit contains Zimmer Dermatome Blades which were recalled by Zimmer due to 38 complaints received related to skin grafts being thin and non-uniform when using the affected blades.
- **Classification**: Class II
- **Recalling firm**: ROi CPS LLC
- **Quantity**: 103 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0070-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0070-2024%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 10194717113805, Lot Number 97289, Exp Date 2025-07-16 |

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

## Distribution

Missouri

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

- [Missouri](https://isitonrecall.com/state/missouri/)

## Dates in the source

- **Report date**: Oct 11, 2023
- **Recall initiation date**: Sep 11, 2023
- **Center classification date**: Oct 5, 2023

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-0070-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [ROi CPS LLC records](https://isitonrecall.com/brand/roi-cps-llc/)