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.

Other recalls by Zimmer Surgical

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• Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Dual Hose with CPC Connectors Model/Catalog Number: 60…
  FDA Device · Class II · 2026-07-08 · Zimmer Surgical
• Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100 Software Version: S…
  FDA Device · Class II · 2026-02-04 · Zimmer Surgical
• Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 60500010100 Software Version: S…
  FDA Device · Class II · 2026-02-04 · Zimmer Surgical
• Zimmer Dermatome AN, Model/Catalog Number: 88710100
  FDA Device · Class II · 2025-12-24 · Zimmer Surgical

All Zimmer Surgical recalls

Source

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

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.