Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100 Software Version: Software version v2.06 or prior are within scope of the recall for A.T.S.¿ 3200TS Product Description: A.T.S 3200TS Tourniquet Systems Component: N/A
Reported: February 4, 2026 Initiated: December 24, 2025 #Z-1202-2026
Product Description
Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100 Software Version: Software version v2.06 or prior are within scope of the recall for A.T.S.¿ 3200TS Product Description: A.T.S 3200TS 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
- 51
- 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.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100 Software Version: Software version v2.06 or prior are within scope of the recall for A.T.S.¿ 3200TS Product Description: A.T.S 3200TS Tourniquet Systems Component: N/A. Recalled by Zimmer Surgical Inc. Units affected: 51.
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-1202-2026.
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