# FDA recall Z-1202-2026

> **Zimmer Surgical Inc** · Class II · device recall initiated 2025-12-24.

## Product

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.

## Distribution

International distribution to the countries of Canada and EMEA only.

## Key facts

- **Recall number:** Z-1202-2026
- **Recalling firm:** Zimmer Surgical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-24
- **Report date:** 2026-02-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dover, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1202-2026

## Citation

> AI Analytics. FDA recall Z-1202-2026. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1202-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*