# FDA recall Z-1802-2020

> **Stryker Sustainability Solutions** · Class II · device recall initiated 2019-10-09.

## Product

Zimmer Tourniquet Cuff 30" (Blue), PLC Dual Port, Single Bladder, Item Number: 60-7070-105, UDI: 00885825013868, Reprocessed Tourniquet Cuff - Product Usage: Reprocessed tourniquet cuffs are indicated for use in patients who require surgery of the extremities with an expected duration of less than 90 minutes when temporary exsanguination of a limb is desired.

## Reason for recall

Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device misuse during procedure (2) Inadequate Limb Compression Force.

## Distribution

US Nationwide distribution including the states of  SC, TX, UT, NY, AR

## Key facts

- **Recall number:** Z-1802-2020
- **Recalling firm:** Stryker Sustainability Solutions
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-09
- **Report date:** 2020-05-06
- **Termination date:** 2021-01-14

- **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-1802-2020

## Citation

> AI Analytics. FDA recall Z-1802-2020. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-1802-2020. Source: US FDA. Licensed CC0.

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