Zimmer Surgical Inc: Device Recall

Recall #Z-1201-2026 · 12/24/2025

Class II: Risk

Recall Details

Recall Number: Z-1201-2026
Classification: Class II
Product Type: Device
Recalling Firm: Zimmer Surgical Inc
Status: Ongoing
Date Initiated: 12/24/2025
Location: Dover, OH, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 206

Reason for Recall

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.

Product Description

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

Distribution Pattern

International distribution to the countries of Canada and EMEA only.

Other Recalls by Zimmer Surgical Inc

Class II: Risk 12/24/2025

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: Risk 11/24/2025

The devices may have a misaligned thickness control bar.
Class II: Risk 11/24/2025

The devices may have a misaligned thickness control bar.

View all recalls by Zimmer Surgical Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.