# FDA recall Z-1356-2020

> **Zimmer Surgical Inc** · Class II · device recall initiated 2020-01-03.

## Product

Zimmer Sterile Disposable  Tourniquet Cuff with Protective  Sleeve and PLC, Dual Port, Dual  Bladder, Item No. 60708015200, UDI (01)00889024377547  (17)230812(10)27968701    The product is a tourniquet - Product Usage: Tourniquets are intended to be used by qualified medical professionals to exert enough pressure on the arterial blood flow in a limb to produce a bloodless operating field.

## Reason for recall

When inflating/deflating a single bladder, both bladders could potentially inflate/deflate due to a leak between the bladders.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of CA, FL, IA, ID, IL, LA, MA, MO, NC, NY, OH, OR, PA, SC, TN, TX, WA, WI, and WV and country of Netherlands.

## Key facts

- **Recall number:** Z-1356-2020
- **Recalling firm:** Zimmer Surgical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-01-03
- **Report date:** 2020-03-04
- **Termination date:** 2020-10-30

- **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-1356-2020

## Citation

> AI Analytics. FDA recall Z-1356-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1356-2020. Source: US FDA. Licensed CC0.

---

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