# FDA recall Z-0925-2026

> **Zimmer Surgical Inc** · Class II · device recall initiated 2025-11-24.

## 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

- **Recall number:** Z-0925-2026
- **Recalling firm:** Zimmer Surgical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-11-24
- **Report date:** 2025-12-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dover, OH, United States

## Primary source

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

## Citation

> AI Analytics. FDA recall Z-0925-2026. Retrieved 2026-09-04 from https://api.ai-analytics.org/recall/Z-0925-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*