FDA recall Z-0925-2026

Product

Zimmer Dermatome AN, Model/Catalog Number: 88710100

Reason for recall

The devices may have a misaligned thickness control bar.

Distribution

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.

Key facts

Status

Ongoing

Initiation date

2025-11-24

Report date

2025-12-24

Voluntary/Mandated

Voluntary: Firm initiated

Location

Dover, OH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0925-2026