Medical device recalls Moderate risk

Zimmer Surgical Inc recalls Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 60500010100…

Recall date
December 24, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1201-2026
FDA classification
Class II
Brand / firm
Zimmer Surgical Inc
Sold / distributed
International distribution to the countries of Canada and EMEA only.

Why it was recalled

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 means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 60500010100 Software Version: Software version v2.04 or prior are within scope of the recall for A.T.S.¿ 5000TS Product Description: A.T.S 5000TS Tourniquet Systems Component: N/A

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