FDA Device recall Z-0069-2024

Zimmer Dermatome Blades- 10-pack boxes of blades

• FDA Device
• Class II
• ongoing
• Published 2023-10-11

On 2023-10-11 the FDA classified a Class II recall of Zimmer Dermatome Blades- 10-pack boxes of blades by Zimmer Surgical, citing 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….

Read the official FDA Device notice

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

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

Identifiers

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0069-2024%22

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