# FDA recall Z-2673-2026

> **Zimmer Surgical Inc** · Class II · device recall initiated 2026-06-09.

## Product

Brand Name: Sterile Tourniquet Hoses  Product Name: A.T.S¿ 4000 TS Tourniquet Systems Dual Hose with CPC Connectors  Model/Catalog Number: 60-1812-101-00  Software Version: N/A  Product Description: Dual Sterile Extension Hose with PLC Connector  Component: N/A

## Reason for recall

Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find another readily available device.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada and EMEA.

## Key facts

- **Recall number:** Z-2673-2026
- **Recalling firm:** Zimmer Surgical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-09
- **Report date:** 2026-07-08

- **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-2673-2026

## Citation

> MORVS. FDA recall Z-2673-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2673-2026. Source: US FDA. Licensed CC0.

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