PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: February 4, 2026 Initiated: December 24, 2025 #Z-1201-2026

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

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.

Details

Recalling Firm
Zimmer Surgical Inc
Units Affected
206
Distribution
International distribution to the countries of Canada and EMEA only.
Location
Dover, OH

Frequently Asked Questions

What product 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. Recalled by Zimmer Surgical Inc. Units affected: 206.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 4, 2026. Severity: Moderate. Recall number: Z-1201-2026.