# FDA recall Z-2405-2024

> **Stryker Sustainability Solutions** · Class II · device recall initiated 2024-05-31.

## Product

REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly

## Reason for recall

Mislabeling; tourniquet cuff packaging  labeled as dual port single bladder  but contains a tourniquet cuff single port single bladder.

## Distribution

US Nationwide distribution in the states of CA, CO, IL, MI, OR, WI.

## Key facts

- **Recall number:** Z-2405-2024
- **Recalling firm:** Stryker Sustainability Solutions
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-31
- **Report date:** 2024-07-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tempe, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2405-2024

## Citation

> AI Analytics. FDA recall Z-2405-2024. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-2405-2024. Source: US FDA. Licensed CC0.

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