# FDA recall Z-2053-2019

> **Zevex Incorporated (dba MOOG Medical Devices Group)** · Class II · device recall initiated 2019-02-27.

## Product

MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carton, 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

Administration sets leaked at the filter.

## Distribution

Distribution was made to GA, IL, KS, MA, MI, and OH.  There was no foreign/military/government distribution.

## Key facts

- **Recall number:** Z-2053-2019
- **Recalling firm:** Zevex Incorporated (dba MOOG Medical Devices Group)
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-02-27
- **Report date:** 2019-07-31
- **Termination date:** 2021-04-28

- **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-2053-2019

## Citation

> AI Analytics. FDA recall Z-2053-2019. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2053-2019. Source: US FDA. Licensed CC0.

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