Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Zimmer Air Dermatome Recalled by Zimmer Surgical Inc Due to The devices may have a misaligned thickness control...

Date: November 24, 2025
Company: Zimmer Surgical Inc
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer Surgical Inc directly.

Affected Products

Zimmer Air Dermatome, Model/Catalog Number: 00880100100

Quantity: 839 units

Why Was This Recalled?

The devices may have a misaligned thickness control bar.

Where Was This Sold?

Distribution regions: USA, Hong Kong, Thailand, Japan, Korea, Australia, Taiwan, India, Malaysia, Singapore, China, Canada, EMEA, Mexico, Trinidad & Tobago, Panama, Guatemala Refer to the attached ZFA 2025-00141_Initial Consignee List and ZFA 2025-001141_Initial Distribution History containing the distribution and the identification of the domestic consignees.

About Zimmer Surgical Inc

Zimmer Surgical Inc has 26 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report