# FDA recall Z-0701-2018

> **Zevex Incorporated (dba Moog Medical Medical Devices Group)** · Class II · device recall initiated 2017-11-10.

## Product

MOOG Curlin Infusion Administration Set, Ref 340-4168, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Female Luer Y-Site with Check Valve, Anti-Siphon Valve included for Free Flow Protection, packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile.      Product Usage:  Administration set to be used with the Moog Curlin infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.

## Reason for recall

Particulate found on the Curlin spike.

## Distribution

Distribution was nationwide.  There was government and military distribution.  Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.

## Key facts

- **Recall number:** Z-0701-2018
- **Recalling firm:** Zevex Incorporated (dba Moog Medical Medical Devices Group)
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-11-10
- **Report date:** 2018-03-07
- **Termination date:** 2018-12-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Salt Lake City, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0701-2018

## Citation

> AI Analytics. FDA recall Z-0701-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0701-2018. Source: US FDA. Licensed CC0.

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