Recall Z-0924-2026— Zimmer Surgical Inc
Class II · Ongoing
Class II FDA medical device recall by Zimmer Surgical Inc, initiated 2025-11-24. FDA's recall record names no specific 510(k) clearance for this event. Product: Zimmer Air Dermatome, Model/Catalog Number: 00880100100. Reason: The devices may have a misaligned thickness control bar..
- Recalling firm
- Zimmer Surgical Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-11-24
- Firm location
- Dover, OH, United States
Product description
Zimmer Air Dermatome, Model/Catalog Number: 00880100100
Reason for recall
The devices may have a misaligned thickness control bar.
Data sourced from openFDA. This site is unofficial and independent of the FDA.