Zimmer Surgical Inc: Device Recall

Recall #Z-0925-2026 · 11/24/2025

Class II: Risk

Recall Details

Recall Number: Z-0925-2026
Classification: Class II
Product Type: Device
Recalling Firm: Zimmer Surgical Inc
Status: Ongoing
Date Initiated: 11/24/2025
Location: Dover, OH, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 498 units

Reason for Recall

The devices may have a misaligned thickness control bar.

Product Description

Zimmer Dermatome AN, Model/Catalog Number: 88710100

Distribution Pattern

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.

Other Recalls by Zimmer Surgical Inc

Class II: Risk 12/24/2025

Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.
Class II: Risk 12/24/2025

Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.
Class II: Risk 11/24/2025

The devices may have a misaligned thickness control bar.

View all recalls by Zimmer Surgical Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.