# FDA recall Z-0069-2024

> **Zimmer Surgical Inc** · Class II · device recall initiated 2023-09-05.

## Product

Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the dermatome handpiece which is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities  Part number: 00880000010

## Reason for recall

Skin grafts thin and non-uniform when using the affected blades. The issue would be identified at the time of use and may result in the need for additional harvests to adequately cover the area

## Distribution

US Nationwide Foreign:  AUSTRALIA BRAZIL CHINA HONG KONG INDIA JAPAN MALAYSIA MEXICO NETHERLANDS ON SEOUL SINGAPORE TAIWAN THAILAND

## Key facts

- **Recall number:** Z-0069-2024
- **Recalling firm:** Zimmer Surgical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-05
- **Report date:** 2023-10-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dover, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0069-2024

## Citation

> AI Analytics. FDA recall Z-0069-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0069-2024. Source: US FDA. Licensed CC0.

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