FDA recall record · openFDA

Zimmer Surgical Inc

6 FDA recalls on record (2023–2025) — 6 device. 6 still ongoing.

Class I (most serious)

Class II

Class III

ongoing

How to read this. A recall count is not a quality verdict — large manufacturers recall more simply by volume, and a voluntary recall is the safety system working as intended. The signal to weight is the Class I count (the FDA's most-serious tier — reasonable probability of serious harm or death) and whether recalls are still ongoing. Most recalls are Class II/III. "Ongoing" reflects openFDA's last-published status — device recalls often stay marked ongoing long after they're resolved in practice; confirm current status at the FDA.

Most common reasons

The devices may have a misaligned thickness control bar. 2

Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language 2

Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridge pattern is a 1.5:1 ratio. The problem may 1

Skin grafts thin and non-uniform when using the affected blades. The issue would be identified at the time of use and ma 1

Recalls

Zimmer Air Dermatome, Model/Catalog Number: 00880100100 Class II 2025-11-24 Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 6032001010 Class II 2025-12-24 Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 6050001010 Class II 2025-12-24 Zimmer Dermatome AN, Model/Catalog Number: 88710100 Class II 2025-11-24 3:1 Dermacarrier, Model Number 00219501300, skin graft carrier Class II 2024-01-02 Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the dermatome handpiece which is a skin grafting Class II 2023-09-05

RECORDED — these are the FDA's published recall enforcement records (openFDA). Recalls are listed under the exact firm name as filed; a large manufacturer may also file under name variants, so this may not be the company's complete cross-variant record — confirm at the FDA recall database. This page informs and routes; it is not medical advice or a verdict on the company.

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