# FDA recall Z-2722-2017

> **ICU Medical, Inc.** · Class II · device recall initiated 2017-05-30.

## Product

10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold (Orange, Red, Blue, Purple, Yellow Rings), Check Valve, Clamp, Rotating Luer.   Product Usage:  The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein).

## Reason for recall

The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak.

## Distribution

Distribution to Italy and France, and  the following states in the US: AZ, OH, TX, WA.

## Key facts

- **Recall number:** Z-2722-2017
- **Recalling firm:** ICU Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-30
- **Report date:** 2017-07-19
- **Termination date:** 2024-09-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Clemente, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2722-2017

## Citation

> AI Analytics. FDA recall Z-2722-2017. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-2722-2017. Source: US FDA. Licensed CC0.

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